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
8,177
archived clinical trials in
Orthopedic

Evaluation of the Duration of Bupivacaine Spinal Block in Orthopedic Procedures With and Without Epinephrine Wash
Evaluation of the Duration of Bupivacaine Spinal Block as the Primary Anesthetic for Orthopedic Procedures With and Without Epinephrine Wash
Status: Enrolling
Updated:  12/31/1969
2184
mi
from 91732
Charleston, SC
Evaluation of the Duration of Bupivacaine Spinal Block in Orthopedic Procedures With and Without Epinephrine Wash
Evaluation of the Duration of Bupivacaine Spinal Block as the Primary Anesthetic for Orthopedic Procedures With and Without Epinephrine Wash
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina
2184
mi
from 91732
Charleston, SC
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Fibular Fixation in Ankle Fractures:Plate Verses Nail.
Fibular Fixation in Ankle Fractures: a Randomized-Controlled Trial Comparing Plating Versus Intramedullary Nailing
Status: Enrolling
Updated:  12/31/1969
2184
mi
from 91732
Orlando, FL
Fibular Fixation in Ankle Fractures:Plate Verses Nail.
Fibular Fixation in Ankle Fractures: a Randomized-Controlled Trial Comparing Plating Versus Intramedullary Nailing
Status: Enrolling
Updated: 12/31/1969
Orlando Health
2184
mi
from 91732
Orlando, FL
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Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
A Prospective, Multi-Center, Non-Randomized Study to Assess Clinical Outcomes Using Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior Lumbar Interbody Fusion or Lateral Lumbar Interbody Fusion
Status: Enrolling
Updated:  12/31/1969
1879
mi
from 91732
Cincinnati, OH
Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
A Prospective, Multi-Center, Non-Randomized Study to Assess Clinical Outcomes Using Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior Lumbar Interbody Fusion or Lateral Lumbar Interbody Fusion
Status: Enrolling
Updated: 12/31/1969
Carl & Edyth Lindner Center for Research The Christ Hospital
1879
mi
from 91732
Cincinnati, OH
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Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
A Prospective, Multi-Center, Non-Randomized Study to Assess Clinical Outcomes Using Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior Lumbar Interbody Fusion or Lateral Lumbar Interbody Fusion
Status: Enrolling
Updated:  12/31/1969
2177
mi
from 91732
Niagara Falls, NY
Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
A Prospective, Multi-Center, Non-Randomized Study to Assess Clinical Outcomes Using Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior Lumbar Interbody Fusion or Lateral Lumbar Interbody Fusion
Status: Enrolling
Updated: 12/31/1969
Spine Surgery of Buffalo Niagara
2177
mi
from 91732
Niagara Falls, NY
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Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
A Prospective, Multi-Center, Non-Randomized Study to Assess Clinical Outcomes Using Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior Lumbar Interbody Fusion or Lateral Lumbar Interbody Fusion
Status: Enrolling
Updated:  12/31/1969
2189
mi
from 91732
Williamsville, NY
Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
A Prospective, Multi-Center, Non-Randomized Study to Assess Clinical Outcomes Using Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior Lumbar Interbody Fusion or Lateral Lumbar Interbody Fusion
Status: Enrolling
Updated: 12/31/1969
AXIS Neurosurgery and Spine of WNY, PLLC
2189
mi
from 91732
Williamsville, NY
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Effectiveness of KneeMD on Flexion Contracture in Total Knee Arthroplasty Patients
A Prospective Randomized Trial to Examine the Effectiveness of KneeMD on Flexion Contracture in Total Knee Arthroplasty Patients
Status: Enrolling
Updated:  12/31/1969
2309
mi
from 91732
Annapolis, MD
Effectiveness of KneeMD on Flexion Contracture in Total Knee Arthroplasty Patients
A Prospective Randomized Trial to Examine the Effectiveness of KneeMD on Flexion Contracture in Total Knee Arthroplasty Patients
Status: Enrolling
Updated: 12/31/1969
Anne Arundel Medical Center
2309
mi
from 91732
Annapolis, MD
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Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries
Comparing Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol Administration for Carpal Tunnel Release and Distal Radius Fracture Surgeries
Status: Enrolling
Updated:  12/31/1969
2147
mi
from 91732
Pittsburgh, PA
Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries
Comparing Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol Administration for Carpal Tunnel Release and Distal Radius Fracture Surgeries
Status: Enrolling
Updated: 12/31/1969
Kaufmann Building
2147
mi
from 91732
Pittsburgh, PA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
328
mi
from 91732
Palo Alto, CA
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Pediatric Neuromuscular Clinic Stanford University
328
mi
from 91732
Palo Alto, CA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
1332
mi
from 91732
Kansas City, KA
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
University of Kansas Medical Center
1332
mi
from 91732
Kansas City, KA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
1960
mi
from 91732
Columbus, OH
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
The Ohio State University, Wexner Medical Center
1960
mi
from 91732
Columbus, OH
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
2302
mi
from 91732
Baltimore, MD
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Hospital Institute for Clinical and Translational Research Pediatric Clinical Research Unit
2302
mi
from 91732
Baltimore, MD
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
570
mi
from 91732
Salt Lake City, UT
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
The University of Utah, Clinical Neurosciences Center
570
mi
from 91732
Salt Lake City, UT
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
2578
mi
from 91732
Boston, MA
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Boston Children's Hospital
2578
mi
from 91732
Boston, MA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
2491
mi
from 91732
New Britain, CT
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Hospital for Special Care
2491
mi
from 91732
New Britain, CT
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
2184
mi
from 91732
Orlando, FL
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Nemours Children's Hospital
2184
mi
from 91732
Orlando, FL
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
25
mi
from 91732
Los Angeles, CA
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
UCLA
25
mi
from 91732
Los Angeles, CA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
1729
mi
from 91732
Chicago, IL
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Ann & Robert H. Lurie Children's Hospital of Chicago
1729
mi
from 91732
Chicago, IL
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
1569
mi
from 91732
Saint Louis, MO
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Washington University School of Medicine
1569
mi
from 91732
Saint Louis, MO
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
1190
mi
from 91732
Calgary,
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Alberta Children's Hospital
1190
mi
from 91732
Calgary,
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
2203
mi
from 91732
Durham, NC
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
2203
mi
from 91732
Durham, NC
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
2375
mi
from 91732
Philadelphia, PA
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Children's Hospital of Philadelphia
2375
mi
from 91732
Philadelphia, PA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
21
mi
from 91732
Orange, CA
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
The University of California Irvine
21
mi
from 91732
Orange, CA
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A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated:  12/31/1969
825
mi
from 91732
Aurora, CO
A Study of CK-2127107 in Patients With Spinal Muscular Atrophy
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Study of CK-2127107 in Two Ascending Dose Cohorts of Patients With Spinal Muscular Atrophy (SMA)
Status: Enrolling
Updated: 12/31/1969
Children's Hospital Colorado
825
mi
from 91732
Aurora, CO
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interACTION: A Portable Joint Function Monitoring and Training System for Remote Rehabilitation Following TKA
interACTION: A Portable Joint Function Monitoring and Training System for Remote Rehabilitation Following Total Knee Arthroplasty
Status: Enrolling
Updated:  12/31/1969
2121
mi
from 91732
Pittsburgh, PA
interACTION: A Portable Joint Function Monitoring and Training System for Remote Rehabilitation Following TKA
interACTION: A Portable Joint Function Monitoring and Training System for Remote Rehabilitation Following Total Knee Arthroplasty
Status: Enrolling
Updated: 12/31/1969
University of Pittsburgh
2121
mi
from 91732
Pittsburgh, PA
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
59
mi
from 91732
Murrieta, CA
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
Advanced Neurosurgery Associates
59
mi
from 91732
Murrieta, CA
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
356
mi
from 91732
San Francisco, CA
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
University of California at San Francisco (UCSF)
356
mi
from 91732
San Francisco, CA
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
2239
mi
from 91732
Melbourne, FL
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
The BACK Center
2239
mi
from 91732
Melbourne, FL
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
2136
mi
from 91732
Tampa, FL
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
Foundation for Orthopaedic Research and Education (FORE)
2136
mi
from 91732
Tampa, FL
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
2434
mi
from 91732
New York, NY
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
NewYork-Presbyterian/The Allen Hospital
2434
mi
from 91732
New York, NY
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
2117
mi
from 91732
Pittsburgh, PA
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
Alleghany Health Network Research Institute
2117
mi
from 91732
Pittsburgh, PA
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OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated:  12/31/1969
5606
mi
from 91732
Brussels,
OLIF25™ /OLIF51™ Study
A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach
Status: Enrolling
Updated: 12/31/1969
Ste Elisabeth hospital
5606
mi
from 91732
Brussels,
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
2102
mi
from 91732
Charlotte, NC
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
2102
mi
from 91732
Charlotte, NC
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1227
mi
from 91732
Plano, TX
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1227
mi
from 91732
Plano, TX
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
99
mi
from 91732
La Jolla, CA
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
99
mi
from 91732
La Jolla, CA
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
26
mi
from 91732
Santa Monica, CA
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
26
mi
from 91732
Santa Monica, CA
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1728
mi
from 91732
Evanston, IL
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1728
mi
from 91732
Evanston, IL
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1793
mi
from 91732
Carmel, IN
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1793
mi
from 91732
Carmel, IN
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1401
mi
from 91732
Shreveport, LA
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1401
mi
from 91732
Shreveport, LA
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1220
mi
from 91732
Addison, TX
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
1220
mi
from 91732
Addison, TX
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1315
mi
from 91732
Tyler, TX
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1315
mi
from 91732
Tyler, TX
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
822
mi
from 91732
Thornton, CO
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
822
mi
from 91732
Thornton, CO
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
2148
mi
from 91732
Sarasota, FL
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
2148
mi
from 91732
Sarasota, FL
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
2191
mi
from 91732
Lockport, NY
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
2191
mi
from 91732
Lockport, NY
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
2264
mi
from 91732
Reston, VA
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
2264
mi
from 91732
Reston, VA
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
21
mi
from 91732
Orange, CA
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
21
mi
from 91732
Orange, CA
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
1659
mi
from 91732
Paducah, KY
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1659
mi
from 91732
Paducah, KY
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Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated:  12/31/1969
2409
mi
from 91732
Egg Harbor Township, NJ
Investigation of the Simplify® Cervical Artificial Disc
Clinical Study Protocol for the Investigation Of The Simplify® Cervical Artificial Disc
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
2409
mi
from 91732
Egg Harbor Township, NJ
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Study of Opioid Use After Lumbar and Cervical Spine Surgery
The Effect of a Brief Pre-operative Pain Medication Educational Video on Post-operative Prescriptoin Opioid Medication Use in Patients Undergoing Spine Surgery. A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
1190
mi
from 91732
San Antonio, TX
Study of Opioid Use After Lumbar and Cervical Spine Surgery
The Effect of a Brief Pre-operative Pain Medication Educational Video on Post-operative Prescriptoin Opioid Medication Use in Patients Undergoing Spine Surgery. A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Brooke Army Medical Center
1190
mi
from 91732
San Antonio, TX
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A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
Status: Enrolling
Updated:  12/31/1969
804
mi
from 91732
Colorado Springs, CO
A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
804
mi
from 91732
Colorado Springs, CO
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A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
Status: Enrolling
Updated:  12/31/1969
1225
mi
from 91732
Richardson, TX
A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
A Multi-Site Evaluation of the Pain Relief, Support, Fit and Comfort From Use of a Custom Knee or Ankle Brace in Persons Suffering From Chronic Ankle or Knee Pain and Instability
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
1225
mi
from 91732
Richardson, TX
Click here to add this to my saved trials