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
Medical University of South Carolina
mi
from
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
mi
from
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
Orlando Health
mi
from
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
mi
from
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
Carl & Edyth Lindner Center for Research The Christ Hospital
mi
from
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
mi
from
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
Spine Surgery of Buffalo Niagara
mi
from
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
mi
from
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
AXIS Neurosurgery and Spine of WNY, PLLC
mi
from
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
mi
from
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
Anne Arundel Medical Center
mi
from
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
mi
from
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
Kaufmann Building
mi
from
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
mi
from
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
Pediatric Neuromuscular Clinic Stanford University
mi
from
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
mi
from
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
University of Kansas Medical Center
mi
from
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
mi
from
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
The Ohio State University, Wexner Medical Center
mi
from
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
mi
from
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
Johns Hopkins Hospital Institute for Clinical and Translational Research Pediatric Clinical Research Unit
mi
from
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
mi
from
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
The University of Utah, Clinical Neurosciences Center
mi
from
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
mi
from
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
Boston Children's Hospital
mi
from
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
mi
from
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
Hospital for Special Care
mi
from
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
mi
from
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
Nemours Children's Hospital
mi
from
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
mi
from
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
UCLA
mi
from
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
mi
from
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
Ann & Robert H. Lurie Children's Hospital of Chicago
mi
from
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
mi
from
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
Washington University School of Medicine
mi
from
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
mi
from
Saint Louis, MO
Click here to add this to my saved trials
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
mi
from
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
mi
from
Calgary,
Click here to add this to my saved trials
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
mi
from
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
mi
from
Durham, NC
Click here to add this to my saved trials
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
mi
from
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
mi
from
Philadelphia, PA
Click here to add this to my saved trials
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
mi
from
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
mi
from
Orange, CA
Click here to add this to my saved trials
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
mi
from
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
mi
from
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
University of Pittsburgh
mi
from
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
mi
from
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
Advanced Neurosurgery Associates
mi
from
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
mi
from
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
University of California at San Francisco (UCSF)
mi
from
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)
mi
from
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
The BACK Center
mi
from
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
mi
from
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
Foundation for Orthopaedic Research and Education (FORE)
mi
from
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)
mi
from
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
NewYork-Presbyterian/The Allen Hospital
mi
from
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
mi
from
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
Alleghany Health Network Research Institute
mi
from
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
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
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
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
mi
from
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
mi
from
Addison, TX
Click here to add this to my saved trials
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
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Brooke Army Medical Center
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
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
Clinical Research Facility
mi
from
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
mi
from
Richardson, TX
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