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

Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
Lutheran Medical Center
2432
mi
from 91732
Brooklyn, NY
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
Lutheran Medical Center
2432
mi
from 91732
Brooklyn, NY
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Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
Carolinas Medical Center
2101
mi
from 91732
Charlotte, NC
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
Carolinas Medical Center
2101
mi
from 91732
Charlotte, NC
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Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
Ohio Health Research Center
1960
mi
from 91732
Columbus, OH
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
Ohio Health Research Center
1960
mi
from 91732
Columbus, OH
Click here to add this to my saved trials
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
University of Oklahoma
1165
mi
from 91732
Oklahoma City, OK
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
University of Oklahoma
1165
mi
from 91732
Oklahoma City, OK
Click here to add this to my saved trials
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
Geisinger Clinic
2265
mi
from 91732
Danville, PA
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
Geisinger Clinic
2265
mi
from 91732
Danville, PA
Click here to add this to my saved trials
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
University of Tennessee College of Medicine
1853
mi
from 91732
Chattanooga, TN
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
University of Tennessee College of Medicine
1853
mi
from 91732
Chattanooga, TN
Click here to add this to my saved trials
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated:  8/2/2012
Vanderbilt University Medical Center
1762
mi
from 91732
Nashville, TN
Tibial Delayed Healing Pivotal Clinical Trial
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Status: Enrolling
Updated: 8/2/2012
Vanderbilt University Medical Center
1762
mi
from 91732
Nashville, TN
Click here to add this to my saved trials
Development and Validation of Intraoperative Image-quality Criteria
Development and Validation of Intraoperative Image-quality Criteria A Retrospective Multicenter Case Series to Validate a Set of Intraoperative Image-quality Criteria
Status: Enrolling
Updated:  8/6/2012
Hospital of the University of Pennsylvania
2373
mi
from 91732
Philadelphia, PA
Development and Validation of Intraoperative Image-quality Criteria
Development and Validation of Intraoperative Image-quality Criteria A Retrospective Multicenter Case Series to Validate a Set of Intraoperative Image-quality Criteria
Status: Enrolling
Updated: 8/6/2012
Hospital of the University of Pennsylvania
2373
mi
from 91732
Philadelphia, PA
Click here to add this to my saved trials
Plating of Distal Femur Fractures by Far Cortical Locking Using MotionLoc Screws
MotionLoc Study: Healing of Distal Femur Fractures Stabilized With a Flexible Plating Construct Using MotionLoc Screws
Status: Enrolling
Updated:  8/16/2012
Legacy Health System
829
mi
from 91732
Portland, OR
Plating of Distal Femur Fractures by Far Cortical Locking Using MotionLoc Screws
MotionLoc Study: Healing of Distal Femur Fractures Stabilized With a Flexible Plating Construct Using MotionLoc Screws
Status: Enrolling
Updated: 8/16/2012
Legacy Health System
829
mi
from 91732
Portland, OR
Click here to add this to my saved trials
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated:  8/29/2012
Florida Hospital
2185
mi
from 91732
Orlando, FL
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated: 8/29/2012
Florida Hospital
2185
mi
from 91732
Orlando, FL
Click here to add this to my saved trials
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated:  8/29/2012
Neurological Surgery of Southern Illinois
1584
mi
from 91732
Belleville, IL
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated: 8/29/2012
Neurological Surgery of Southern Illinois
1584
mi
from 91732
Belleville, IL
Click here to add this to my saved trials
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated:  8/29/2012
Indiana Orthopedic Center
1793
mi
from 91732
Indianapolis, IN
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated: 8/29/2012
Indiana Orthopedic Center
1793
mi
from 91732
Indianapolis, IN
Click here to add this to my saved trials
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated:  8/29/2012
Las Cruces Orthopaedic Associates
657
mi
from 91732
Las Cruces, NM
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated: 8/29/2012
Las Cruces Orthopaedic Associates
657
mi
from 91732
Las Cruces, NM
Click here to add this to my saved trials
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated:  8/29/2012
Upstate Bone and Joint Center
2323
mi
from 91732
East Syracuse, NY
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated: 8/29/2012
Upstate Bone and Joint Center
2323
mi
from 91732
East Syracuse, NY
Click here to add this to my saved trials
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated:  8/29/2012
Scott and White Healthcare
1211
mi
from 91732
Temple, TX
CopiOs Posterolateral Fusion Procedure
A Prospective Study Assessing Clinical Outcomes and Radiographic Results After the Use of CopiOs(R) Bone Void Filler (BVF)Sponge in a Posterolateral Fusion Procedure (PLF).
Status: Enrolling
Updated: 8/29/2012
Scott and White Healthcare
1211
mi
from 91732
Temple, TX
Click here to add this to my saved trials
Efficacy and Safety of Xiaflex Injection for Treatment of Dupuytren's Contracture of the Thumb
The Efficacy and Safety of Xiaflex Injections for the Treatment of Thumb Cords in Dupuytren's Contractures
Status: Enrolling
Updated:  9/11/2012
Indiana Hand to Shoulder Center
1792
mi
from 91732
Indianaplis, IN
Efficacy and Safety of Xiaflex Injection for Treatment of Dupuytren's Contracture of the Thumb
The Efficacy and Safety of Xiaflex Injections for the Treatment of Thumb Cords in Dupuytren's Contractures
Status: Enrolling
Updated: 9/11/2012
Indiana Hand to Shoulder Center
1792
mi
from 91732
Indianaplis, IN
Click here to add this to my saved trials
The Value of Traction in the Treatment of Cervical Radiculopathy
The Value of Mechanical Traction in the Treatment of Cervical Radiculopathy
Status: Enrolling
Updated:  9/11/2012
Intermountain Healthcare, Rehab Agency
565
mi
from 91732
Salt Lake City, UT
The Value of Traction in the Treatment of Cervical Radiculopathy
The Value of Mechanical Traction in the Treatment of Cervical Radiculopathy
Status: Enrolling
Updated: 9/11/2012
Intermountain Healthcare, Rehab Agency
565
mi
from 91732
Salt Lake City, UT
Click here to add this to my saved trials
The Value of Traction in the Treatment of Cervical Radiculopathy
The Value of Mechanical Traction in the Treatment of Cervical Radiculopathy
Status: Enrolling
Updated:  9/11/2012
Wilford Hall Medical Center
1182
mi
from 91732
Lackland AFB, TX
The Value of Traction in the Treatment of Cervical Radiculopathy
The Value of Mechanical Traction in the Treatment of Cervical Radiculopathy
Status: Enrolling
Updated: 9/11/2012
Wilford Hall Medical Center
1182
mi
from 91732
Lackland AFB, TX
Click here to add this to my saved trials
Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
A Post Market, Open-Label Study of the Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
Status: Enrolling
Updated:  9/11/2012
Indiana Hand to Shoulder Center
1792
mi
from 91732
Indianaplis, IN
Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
A Post Market, Open-Label Study of the Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
Status: Enrolling
Updated: 9/11/2012
Indiana Hand to Shoulder Center
1792
mi
from 91732
Indianaplis, IN
Click here to add this to my saved trials
Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
A Post Market, Open-Label Study of the Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
Status: Enrolling
Updated:  9/11/2012
Stony Brook University
2503
mi
from 91732
Stony Brook, NY
Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
A Post Market, Open-Label Study of the Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
Status: Enrolling
Updated: 9/11/2012
Stony Brook University
2503
mi
from 91732
Stony Brook, NY
Click here to add this to my saved trials
Multifaceted Treatment of Catheter-related Urinary Tract Infection
Multifaceted Treatment of Catheter-related Urinary Tract Infection
Status: Enrolling
Updated:  10/15/2012
Michael E. DeBakey VA Medical Center (152)
1357
mi
from 91732
Houston, TX
Multifaceted Treatment of Catheter-related Urinary Tract Infection
Multifaceted Treatment of Catheter-related Urinary Tract Infection
Status: Enrolling
Updated: 10/15/2012
Michael E. DeBakey VA Medical Center (152)
1357
mi
from 91732
Houston, TX
Click here to add this to my saved trials
Early Aggressive Pain Management is Associated With Improved Outcomes in Blunt Thoracic Trauma
Early Aggressive Pain Management is Associated With Improved Outcomes in Blunt Thoracic Trauma
Status: Enrolling
Updated:  10/16/2012
Univ of California, San Francisco/San Francisco General Hosp
353
mi
from 91732
San Francisco, CA
Early Aggressive Pain Management is Associated With Improved Outcomes in Blunt Thoracic Trauma
Early Aggressive Pain Management is Associated With Improved Outcomes in Blunt Thoracic Trauma
Status: Enrolling
Updated: 10/16/2012
Univ of California, San Francisco/San Francisco General Hosp
353
mi
from 91732
San Francisco, CA
Click here to add this to my saved trials
Intervertebral Disc Augmentation With Minimally Invasive Surgical Procedure
Intervertebral Disc Nucleus Augmentation With Allograft Meniscus With Minimally Invasive Surgical Procedure
Status: Enrolling
Updated:  10/16/2012
UF&Shands Orthopaedics and Sports Medicine Institute
2103
mi
from 91732
Gainesville, FL
Intervertebral Disc Augmentation With Minimally Invasive Surgical Procedure
Intervertebral Disc Nucleus Augmentation With Allograft Meniscus With Minimally Invasive Surgical Procedure
Status: Enrolling
Updated: 10/16/2012
UF&Shands Orthopaedics and Sports Medicine Institute
2103
mi
from 91732
Gainesville, FL
Click here to add this to my saved trials
The Addition of a Pilates Program for Short-Term Improvements in Patients With Spondylolysis or Spondylolisthesis
The Addition of a Pilates Program for Short-Term Improvements in Self Report and Physical Functions With Patients With Spondylolysis or Spondylolisthesis: A Randomized Clinical Trial
Status: Enrolling
Updated:  10/17/2012
Akron Children's Hospital Orthopaedic and Sports Physical Therapy Center
2040
mi
from 91732
Akron, OH
The Addition of a Pilates Program for Short-Term Improvements in Patients With Spondylolysis or Spondylolisthesis
The Addition of a Pilates Program for Short-Term Improvements in Self Report and Physical Functions With Patients With Spondylolysis or Spondylolisthesis: A Randomized Clinical Trial
Status: Enrolling
Updated: 10/17/2012
Akron Children's Hospital Orthopaedic and Sports Physical Therapy Center
2040
mi
from 91732
Akron, OH
Click here to add this to my saved trials
Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
In Vivo Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
Status: Enrolling
Updated:  10/25/2012
Porter Adventist Hospital, Colorado Joint Replacement
817
mi
from 91732
Denver, CO
Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
In Vivo Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
Status: Enrolling
Updated: 10/25/2012
Porter Adventist Hospital, Colorado Joint Replacement
817
mi
from 91732
Denver, CO
Click here to add this to my saved trials
Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
In Vivo Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
Status: Enrolling
Updated:  10/25/2012
Science and Engineering Research Facility, The University of Tennessee
1923
mi
from 91732
Knoxville, TN
Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
In Vivo Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
Status: Enrolling
Updated: 10/25/2012
Science and Engineering Research Facility, The University of Tennessee
1923
mi
from 91732
Knoxville, TN
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Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
In Vivo Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
Status: Enrolling
Updated:  10/25/2012
Perkins Hall, The University of Tennessee
1923
mi
from 91732
Knoxville, TN
Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
In Vivo Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA
Status: Enrolling
Updated: 10/25/2012
Perkins Hall, The University of Tennessee
1923
mi
from 91732
Knoxville, TN
Click here to add this to my saved trials
Evaluation of Coronary Luminal Diameter Enlargement With Emerge™ 1.20 mm PTCA Dilatation Catheter
EMERGE: Evaluation of Coronary Luminal Diameter Enlargement With Emerge™ 1.20 mm PTCA Dilatation Catheter
Status: Enrolling
Updated:  10/30/2012
Piedmont Heart Institute
1918
mi
from 91732
Atlanta, GA
Evaluation of Coronary Luminal Diameter Enlargement With Emerge™ 1.20 mm PTCA Dilatation Catheter
EMERGE: Evaluation of Coronary Luminal Diameter Enlargement With Emerge™ 1.20 mm PTCA Dilatation Catheter
Status: Enrolling
Updated: 10/30/2012
Piedmont Heart Institute
1918
mi
from 91732
Atlanta, GA
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
1784
mi
from 91732
Birmingham, AL
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
1784
mi
from 91732
Birmingham, AL
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
105
mi
from 91732
San Diego, CA
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
105
mi
from 91732
San Diego, CA
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
817
mi
from 91732
Denver, CO
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
817
mi
from 91732
Denver, CO
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
1819
mi
from 91732
Anderson, IN
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
1819
mi
from 91732
Anderson, IN
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
1609
mi
from 91732
Duluth, MN
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
1609
mi
from 91732
Duluth, MN
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
1573
mi
from 91732
St Louis, MO
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
1573
mi
from 91732
St Louis, MO
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
2436
mi
from 91732
Bronx, NY
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
2436
mi
from 91732
Bronx, NY
Click here to add this to my saved trials
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated:  11/5/2012
Clinical Research Facility
2356
mi
from 91732
Allentown, PA
Study To Assess Fracture Healing With Sclerostin Antibody
A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults With a Fresh Unilateral Hip Fracture, Status Post Surgical Fixation
Status: Enrolling
Updated: 11/5/2012
Clinical Research Facility
2356
mi
from 91732
Allentown, PA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
1784
mi
from 91732
Birmingham, AL
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
1784
mi
from 91732
Birmingham, AL
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
1775
mi
from 91732
Cullman, AL
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
1775
mi
from 91732
Cullman, AL
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Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
343
mi
from 91732
Phoenix, AZ
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
343
mi
from 91732
Phoenix, AZ
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
353
mi
from 91732
Scottsdale, AZ
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
353
mi
from 91732
Scottsdale, AZ
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
343
mi
from 91732
Phoenix, AZ
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
343
mi
from 91732
Phoenix, AZ
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
426
mi
from 91732
Tucson, AZ
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
426
mi
from 91732
Tucson, AZ
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
22
mi
from 91732
Beverly Hills, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
22
mi
from 91732
Beverly Hills, CA
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Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
82
mi
from 91732
Encinitas, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
82
mi
from 91732
Encinitas, CA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
25
mi
from 91732
Fountain Valley, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
25
mi
from 91732
Fountain Valley, CA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
95
mi
from 91732
La Jolla, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
95
mi
from 91732
La Jolla, CA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Merz Investigative Site #001986
13
mi
from 91732
Los Angeles, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Merz Investigative Site #001986
13
mi
from 91732
Los Angeles, CA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
311
mi
from 91732
Los Gatos, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
311
mi
from 91732
Los Gatos, CA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
31
mi
from 91732
Newport Beach, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
31
mi
from 91732
Newport Beach, CA
Click here to add this to my saved trials
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated:  11/8/2012
Clinical Research Facility
363
mi
from 91732
Sacramento, CA
Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Prospective, Observational Trial Evaluating Xeomin®(incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States
Status: Enrolling
Updated: 11/8/2012
Clinical Research Facility
363
mi
from 91732
Sacramento, CA
Click here to add this to my saved trials