Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
6,666
archived clinical trials in
Hospital

Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Arlington Family Research Center
1205
mi
from 91732
Arlington, TX
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Arlington Family Research Center
1205
mi
from 91732
Arlington, TX
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Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Utah Valley Pediatrics
553
mi
from 91732
Orem, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Utah Valley Pediatrics
553
mi
from 91732
Orem, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
J. Lewis Research Inc./Foothill Family Clininc
572
mi
from 91732
Salt Lake City, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
J. Lewis Research Inc./Foothill Family Clininc
572
mi
from 91732
Salt Lake City, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
J. Lewis Research - FirstMed East
565
mi
from 91732
Salt Lake City, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
J. Lewis Research - FirstMed East
565
mi
from 91732
Salt Lake City, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
J. Lewis Research, Inc. / Foothill Family Clinic South
565
mi
from 91732
Salt Lake City, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
J. Lewis Research, Inc. / Foothill Family Clinic South
565
mi
from 91732
Salt Lake City, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Legacy Point Family Medicine
580
mi
from 91732
West Point, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Legacy Point Family Medicine
580
mi
from 91732
West Point, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Pediatric Research of Charlottesville, LLC
2208
mi
from 91732
Charlottesville, VA
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Pediatric Research of Charlottesville, LLC
2208
mi
from 91732
Charlottesville, VA
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Score Physician Alliance, LLC
2125
mi
from 91732
Saint Petersburg, FL
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Score Physician Alliance, LLC
2125
mi
from 91732
Saint Petersburg, FL
Click here to add this to my saved trials
C1INH Inhibitor Preoperative and Post Kidney Transplant to Prevent DGF & IRI
Assessing Safety and Efficacy of Preoperative and Post-Transplant C1 Inhibitor (Berinert®) vs. Placebo in Recipients of a Renal Allograft From Deceased High Risk Donors and Its Impact on DGF and IRI
Status: Enrolling
Updated:  12/31/1969
Cedars-Sinai Medical Center
13
mi
from 91732
Los Angeles, CA
C1INH Inhibitor Preoperative and Post Kidney Transplant to Prevent DGF & IRI
Assessing Safety and Efficacy of Preoperative and Post-Transplant C1 Inhibitor (Berinert®) vs. Placebo in Recipients of a Renal Allograft From Deceased High Risk Donors and Its Impact on DGF and IRI
Status: Enrolling
Updated: 12/31/1969
Cedars-Sinai Medical Center
13
mi
from 91732
Los Angeles, CA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Barrow Neurological Institute - St. Joseph's Hospital and Medical Center
342
mi
from 91732
Phoenix, AZ
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Barrow Neurological Institute - St. Joseph's Hospital and Medical Center
342
mi
from 91732
Phoenix, AZ
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
USC, Keck School of Medicine
11
mi
from 91732
Los Angeles, CA
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
USC, Keck School of Medicine
11
mi
from 91732
Los Angeles, CA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
University of California, Davis Medical Center
366
mi
from 91732
Sacramento, CA
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
University of California, Davis Medical Center
366
mi
from 91732
Sacramento, CA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Cooper Neurological Institute
2378
mi
from 91732
Camden, NJ
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Cooper Neurological Institute
2378
mi
from 91732
Camden, NJ
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Carolina NeuroSurgery and Spine Associates/Carolinas Rehabilitation
2102
mi
from 91732
Charlotte, NC
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Carolina NeuroSurgery and Spine Associates/Carolinas Rehabilitation
2102
mi
from 91732
Charlotte, NC
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Oregon Health and Science University
827
mi
from 91732
Portland, OR
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Oregon Health and Science University
827
mi
from 91732
Portland, OR
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Vidant Medical Center
2290
mi
from 91732
Greenville, NC
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Vidant Medical Center
2290
mi
from 91732
Greenville, NC
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Allegheny General Hospital
2118
mi
from 91732
Pittsburgh, PA
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Allegheny General Hospital
2118
mi
from 91732
Pittsburgh, PA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Barnes-Jewish Hospital at Washington University Medical Center
1569
mi
from 91732
Saint Louis, MO
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Barnes-Jewish Hospital at Washington University Medical Center
1569
mi
from 91732
Saint Louis, MO
Click here to add this to my saved trials
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated:  12/31/1969
Catholic Medical Center
2555
mi
from 91732
Manchester, NH
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated: 12/31/1969
Catholic Medical Center
2555
mi
from 91732
Manchester, NH
Click here to add this to my saved trials
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated:  12/31/1969
Vanderbilt University Medical Center
1762
mi
from 91732
Nashville, TN
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
1762
mi
from 91732
Nashville, TN
Click here to add this to my saved trials
Effect of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Subacute TBI
Effect of Administration of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Patients With Persistent Symptoms During the Subacute Period After TBI
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center
2277
mi
from 91732
Bethesda, MD
Effect of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Subacute TBI
Effect of Administration of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Patients With Persistent Symptoms During the Subacute Period After TBI
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center
2277
mi
from 91732
Bethesda, MD
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Maricopa Medical Center
347
mi
from 91732
Phoenix, AZ
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Maricopa Medical Center
347
mi
from 91732
Phoenix, AZ
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Colorado at Denver, Teaching
825
mi
from 91732
Aurora, CO
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Colorado at Denver, Teaching
825
mi
from 91732
Aurora, CO
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Iowa Hospitals and Clinics
1528
mi
from 91732
Iowa City, IA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Iowa Hospitals and Clinics
1528
mi
from 91732
Iowa City, IA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Burnett Burn Center at The University of Kansas Hospital
1331
mi
from 91732
Kansas City, KA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Burnett Burn Center at The University of Kansas Hospital
1331
mi
from 91732
Kansas City, KA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
The General Hospital Corporation d/b/a Massachusetts General Hospital
2578
mi
from 91732
Boston, MA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
The General Hospital Corporation d/b/a Massachusetts General Hospital
2578
mi
from 91732
Boston, MA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Emergency Medicine Stony Brook University Hospital
2478
mi
from 91732
Stony Brook, NY
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Emergency Medicine Stony Brook University Hospital
2478
mi
from 91732
Stony Brook, NY
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Lehigh Valley Hospital and Health Network
2357
mi
from 91732
Allentown, PA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Lehigh Valley Hospital and Health Network
2357
mi
from 91732
Allentown, PA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University Hospital, Department of Plastic Surgery
5574
mi
from 91732
Gent,
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University Hospital, Department of Plastic Surgery
5574
mi
from 91732
Gent,
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of South Alabama Department of Surgery
1757
mi
from 91732
Mobile, AL
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of South Alabama Department of Surgery
1757
mi
from 91732
Mobile, AL
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
MedStar Washington Hospital Center
2281
mi
from 91732
Washington,
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
MedStar Washington Hospital Center
2281
mi
from 91732
Washington,
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Florida- Dept. of Surgery
2104
mi
from 91732
Gainesville, FL
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Florida- Dept. of Surgery
2104
mi
from 91732
Gainesville, FL
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A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Joseph M. Still Research Foundation, Inc.
2053
mi
from 91732
Augusta, GA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Joseph M. Still Research Foundation, Inc.
2053
mi
from 91732
Augusta, GA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Johns Hopkins Bayview Medical Center
2304
mi
from 91732
Baltimore, MD
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Bayview Medical Center
2304
mi
from 91732
Baltimore, MD
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
New York-Presbyterian Hospital
2435
mi
from 91732
New York, NY
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
New York-Presbyterian Hospital
2435
mi
from 91732
New York, NY
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Regional Medical Center ,Regional One Health
1587
mi
from 91732
Memphis, TN
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Regional Medical Center ,Regional One Health
1587
mi
from 91732
Memphis, TN
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Texas Medical Branch
1399
mi
from 91732
Galveston, TX
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Texas Medical Branch
1399
mi
from 91732
Galveston, TX
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University Of Utah Hospital
573
mi
from 91732
Salt Lake City, UT
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University Of Utah Hospital
573
mi
from 91732
Salt Lake City, UT
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Harborview Medical Center
961
mi
from 91732
Seattle, WA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Harborview Medical Center
961
mi
from 91732
Seattle, WA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Columbia - St. Mary's
1730
mi
from 91732
Milwaukee, WI
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Columbia - St. Mary's
1730
mi
from 91732
Milwaukee, WI
Click here to add this to my saved trials
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center
2277
mi
from 91732
Bethesda, MD
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center
2277
mi
from 91732
Bethesda, MD
Click here to add this to my saved trials
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass.
Status: Enrolling
Updated:  12/31/1969
Advocate Children's Hospital
1722
mi
from 91732
Oak Lawn, IL
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass.
Status: Enrolling
Updated: 12/31/1969
Advocate Children's Hospital
1722
mi
from 91732
Oak Lawn, IL
Click here to add this to my saved trials
rTMS to Improve Cognitive Function in TBI
Repetitive Transcranial Magnetic Stimulation to Improve Cognitive Function in TBI
Status: Enrolling
Updated:  12/31/1969
VA Palo Alto Health Care System, Palo Alto, CA
327
mi
from 91732
Palo Alto, CA
rTMS to Improve Cognitive Function in TBI
Repetitive Transcranial Magnetic Stimulation to Improve Cognitive Function in TBI
Status: Enrolling
Updated: 12/31/1969
VA Palo Alto Health Care System, Palo Alto, CA
327
mi
from 91732
Palo Alto, CA
Click here to add this to my saved trials
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Status: Enrolling
Updated:  12/31/1969
Northwestern University
1730
mi
from 91732
Chicago, IL
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Status: Enrolling
Updated: 12/31/1969
Northwestern University
1730
mi
from 91732
Chicago, IL
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PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated:  12/31/1969
Naval Medical Center - San Diego
117
mi
from 91732
San Diego, CA
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated: 12/31/1969
Naval Medical Center - San Diego
117
mi
from 91732
San Diego, CA
Click here to add this to my saved trials
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated:  12/31/1969
Walter Reed National Military Medical Center
2277
mi
from 91732
Bethesda, MD
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated: 12/31/1969
Walter Reed National Military Medical Center
2277
mi
from 91732
Bethesda, MD
Click here to add this to my saved trials
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated:  12/31/1969
San Antonio Center for the Intrepid
1188
mi
from 91732
San Antonio, TX
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated: 12/31/1969
San Antonio Center for the Intrepid
1188
mi
from 91732
San Antonio, TX
Click here to add this to my saved trials
Feasibility of Upright Bed Position in ARDS Patients
Feasibility of Upright Bed Position in ARDS Patients
Status: Enrolling
Updated:  12/31/1969
Wake Forest Baptist Health, Medical Intensive Care Unit
2125
mi
from 91732
Winston-Salem, NC
Feasibility of Upright Bed Position in ARDS Patients
Feasibility of Upright Bed Position in ARDS Patients
Status: Enrolling
Updated: 12/31/1969
Wake Forest Baptist Health, Medical Intensive Care Unit
2125
mi
from 91732
Winston-Salem, NC
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Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Status: Enrolling
Updated:  12/31/1969
St. Luke's Rehabilitation Institute
939
mi
from 91732
Spokane, WA
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Status: Enrolling
Updated: 12/31/1969
St. Luke's Rehabilitation Institute
939
mi
from 91732
Spokane, WA
Click here to add this to my saved trials
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Status: Enrolling
Updated:  12/31/1969
Beth Israel Deaconess Medical Center
2578
mi
from 91732
Boston, MA
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Status: Enrolling
Updated: 12/31/1969
Beth Israel Deaconess Medical Center
2578
mi
from 91732
Boston, MA
Click here to add this to my saved trials