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

Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Grand Rapids, MI
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Las Vegas, NV
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Las Vegas, NV
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Brick, NJ
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Brick, NJ
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Albuquerque, NM
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Albuquerque, NM
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Albany, NY
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Albany, NY
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Garden City, NY
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Garden City, NY
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
New York, NY
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
New York, NY
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Oklahoma City, OK
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Bryn Mawr, PA
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Bryn Mawr, PA
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
For information concerning this clinical site, please contact Nymox at 800-936-9669.
mi
from
Sewickley, PA
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
For information concerning this clinical site, please contact Nymox at 800-936-9669.
mi
from
Sewickley, PA
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Memphis, TN
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Memphis, TN
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Houston, TX
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Houston, TX
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
McAllen, TX
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
McAllen, TX
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
San Antonio, TX
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
San Antonio, TX
Click here to add this to my saved trials
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated:  3/9/2017
Clinical Research Facility
mi
from
Richmond, VA
Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018
Phase III Multicenter Prospective Randomized Parallel-Group Placebo-Controlled Double Blind Clinical Evaluation of NX-1207 for the Treatment of BPH NX02-0018
Status: Enrolling
Updated: 3/9/2017
Clinical Research Facility
mi
from
Richmond, VA
Click here to add this to my saved trials
Cardiovascular, Cerebrovascular, and Cognitive Function in Spinal Cord Injury
Cardiovascular, Cerebrovascular, and Cognitive Function in SCI
Status: Enrolling
Updated:  3/9/2017
James J Peters VA Medical Center
mi
from
Bronx, NY
Cardiovascular, Cerebrovascular, and Cognitive Function in Spinal Cord Injury
Cardiovascular, Cerebrovascular, and Cognitive Function in SCI
Status: Enrolling
Updated: 3/9/2017
James J Peters VA Medical Center
mi
from
Bronx, NY
Click here to add this to my saved trials
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Status: Enrolling
Updated:  3/14/2017
Children's Hospital Colorado
mi
from
Aurora, CO
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Status: Enrolling
Updated: 3/14/2017
Children's Hospital Colorado
mi
from
Aurora, CO
Click here to add this to my saved trials
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Status: Enrolling
Updated:  3/14/2017
University of Colorado Hospital
mi
from
Aurora, CO
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Status: Enrolling
Updated: 3/14/2017
University of Colorado Hospital
mi
from
Aurora, CO
Click here to add this to my saved trials
Bimodal Analgesia as Form of Pain Control Post Long Bone Fracture
Bimodal Analgesia as Form of Pain Control Post Long Bone Fracture
Status: Enrolling
Updated:  3/21/2017
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Bimodal Analgesia as Form of Pain Control Post Long Bone Fracture
Bimodal Analgesia as Form of Pain Control Post Long Bone Fracture
Status: Enrolling
Updated: 3/21/2017
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
Comparison of Two Types of Ankle Braces in the Management of Ankle Pain in Hemophilia
Comparison of Two Types of Ankle Braces in the Management of Ankle Pain in Hemophilia
Status: Enrolling
Updated:  4/3/2017
Child Development and Rehabilitation Center, Oregon Health & Science University
mi
from
Portland, OR
Comparison of Two Types of Ankle Braces in the Management of Ankle Pain in Hemophilia
Comparison of Two Types of Ankle Braces in the Management of Ankle Pain in Hemophilia
Status: Enrolling
Updated: 4/3/2017
Child Development and Rehabilitation Center, Oregon Health & Science University
mi
from
Portland, OR
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
St. Joseph's Hospital - Resurgeons Orthopedics
mi
from
Atlanta, GA
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
St. Joseph's Hospital - Resurgeons Orthopedics
mi
from
Atlanta, GA
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Arthritis & Joint Center - U. Mass. Memorial
mi
from
Worcester, MA
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Arthritis & Joint Center - U. Mass. Memorial
mi
from
Worcester, MA
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
PRESSD
mi
from
Southfield, MI
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
PRESSD
mi
from
Southfield, MI
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Montana Neuroscience Institute Foundation
mi
from
Missoula, MT
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Montana Neuroscience Institute Foundation
mi
from
Missoula, MT
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Syracuse Orthopedic Specialists
mi
from
Syracuse, NY
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Syracuse Orthopedic Specialists
mi
from
Syracuse, NY
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Neurosurgical Associates
mi
from
Nashville, TN
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Neurosurgical Associates
mi
from
Nashville, TN
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Brain & Spine of Texas
mi
from
Plano, TX
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Brain & Spine of Texas
mi
from
Plano, TX
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
UCSF
mi
from
San Francisco, CA
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
UCSF
mi
from
San Francisco, CA
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Carrollton Orthopedics
mi
from
Carrollton, GA
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Carrollton Orthopedics
mi
from
Carrollton, GA
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Bluegrass Orthopedics & Hand Care Research
mi
from
Lexington, KY
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Bluegrass Orthopedics & Hand Care Research
mi
from
Lexington, KY
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Henry Ford West Bloomfield Hospital
mi
from
West Bloomfield, MI
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Henry Ford West Bloomfield Hospital
mi
from
West Bloomfield, MI
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Physicians Research Options Spine Center
mi
from
Las Vegas, NV
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Physicians Research Options Spine Center
mi
from
Las Vegas, NV
Click here to add this to my saved trials
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated:  4/4/2017
Buda Health Center
mi
from
Budapest,
Bone Graft Materials Observational Registry
A Prospective Patient Registry for Bone Graft Substitutes in Spinal Fusion: Patient Outcomes and Use in Clinical Practice
Status: Enrolling
Updated: 4/4/2017
Buda Health Center
mi
from
Budapest,
Click here to add this to my saved trials
The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study
The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study
Status: Enrolling
Updated:  4/4/2017
The Christ Hospital
mi
from
Cincinnati, OH
The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study
The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study
Status: Enrolling
Updated: 4/4/2017
The Christ Hospital
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation
Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation
Status: Enrolling
Updated:  4/4/2017
Seattle Medical Research Foundation
mi
from
Seattle, WA
Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation
Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation
Status: Enrolling
Updated: 4/4/2017
Seattle Medical Research Foundation
mi
from
Seattle, WA
Click here to add this to my saved trials
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated:  4/5/2017
Columbia University Medical Center
mi
from
New York, NY
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated: 4/5/2017
Columbia University Medical Center
mi
from
New York, NY
Click here to add this to my saved trials
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated:  4/5/2017
UT Southwestern Medical Center - Children's Medical Center Dallas
mi
from
Dallas, TX
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated: 4/5/2017
UT Southwestern Medical Center - Children's Medical Center Dallas
mi
from
Dallas, TX
Click here to add this to my saved trials
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated:  4/5/2017
University of Utah School of Medicine
mi
from
Salt Lake City, UT
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated: 4/5/2017
University of Utah School of Medicine
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated:  4/5/2017
Children's Hospital Boston
mi
from
Boston, MA
An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)
An Open-label, Escalating Dose Study to Assess the Safety, Tolerability and Dose-range Finding of a Single Intrathecal Dose of ISIS 396443 in Patients With Spinal Muscular Atrophy
Status: Enrolling
Updated: 4/5/2017
Children's Hospital Boston
mi
from
Boston, MA
Click here to add this to my saved trials
Mechanism and Treatment of Sympathetically Maintained Pain
Status: Enrolling
Updated:  4/6/2017
Cleveland Clinic
mi
from
Cleveland, OH
Mechanism and Treatment of Sympathetically Maintained Pain
Status: Enrolling
Updated: 4/6/2017
Cleveland Clinic
mi
from
Cleveland, OH
Click here to add this to my saved trials
Healing With Venlafaxine After Injury (HELP)
Healing With Venlafaxine After Injury: A Randomized Clinical Trial of Venlafaxine Following Motor Vehicle Collision
Status: Enrolling
Updated:  4/12/2017
Spectrum Health
mi
from
Grand Rapids, MI
Healing With Venlafaxine After Injury (HELP)
Healing With Venlafaxine After Injury: A Randomized Clinical Trial of Venlafaxine Following Motor Vehicle Collision
Status: Enrolling
Updated: 4/12/2017
Spectrum Health
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Healing With Venlafaxine After Injury (HELP)
Healing With Venlafaxine After Injury: A Randomized Clinical Trial of Venlafaxine Following Motor Vehicle Collision
Status: Enrolling
Updated:  4/12/2017
Univ of Rochester Medical Center
mi
from
Rochester, NY
Healing With Venlafaxine After Injury (HELP)
Healing With Venlafaxine After Injury: A Randomized Clinical Trial of Venlafaxine Following Motor Vehicle Collision
Status: Enrolling
Updated: 4/12/2017
Univ of Rochester Medical Center
mi
from
Rochester, NY
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Healing With Venlafaxine After Injury (HELP)
Healing With Venlafaxine After Injury: A Randomized Clinical Trial of Venlafaxine Following Motor Vehicle Collision
Status: Enrolling
Updated:  4/12/2017
University of Cincinnati
mi
from
Cincinnati, OH
Healing With Venlafaxine After Injury (HELP)
Healing With Venlafaxine After Injury: A Randomized Clinical Trial of Venlafaxine Following Motor Vehicle Collision
Status: Enrolling
Updated: 4/12/2017
University of Cincinnati
mi
from
Cincinnati, OH
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Electrical Stimulation of the Sphenopalatine Ganglion for the Treatment of Migraine Headaches
Electrical Stimulation of the Sphenopalatine Ganglion for the Treatment of Migraine Headaches
Status: Enrolling
Updated:  4/13/2017
Cleveland Clinic
mi
from
Cleveland, OH
Electrical Stimulation of the Sphenopalatine Ganglion for the Treatment of Migraine Headaches
Electrical Stimulation of the Sphenopalatine Ganglion for the Treatment of Migraine Headaches
Status: Enrolling
Updated: 4/13/2017
Cleveland Clinic
mi
from
Cleveland, OH
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A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated:  4/13/2017
Orange County Neurosurgical Associates
mi
from
Laguna Hills, CA
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated: 4/13/2017
Orange County Neurosurgical Associates
mi
from
Laguna Hills, CA
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A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated:  4/13/2017
Eisenhower Medical Center Desert Orthopedic Center
mi
from
Rancho Mirage, CA
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated: 4/13/2017
Eisenhower Medical Center Desert Orthopedic Center
mi
from
Rancho Mirage, CA
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A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated:  4/13/2017
Yale University
mi
from
New Haven, CT
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated: 4/13/2017
Yale University
mi
from
New Haven, CT
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A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated:  4/13/2017
Rush University Medical Center
mi
from
Chicago, IL
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated: 4/13/2017
Rush University Medical Center
mi
from
Chicago, IL
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A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated:  4/13/2017
Kansas University Medical School
mi
from
Kansas City, KA
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated: 4/13/2017
Kansas University Medical School
mi
from
Kansas City, KA
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A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated:  4/13/2017
Orthopedic Institute of Western KY
mi
from
Paducah, KY
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®
A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP® to Evaluate Long-Term Safety and Efficacy in Patients Requiring 1-2 Level Instrumented PLF
Status: Enrolling
Updated: 4/13/2017
Orthopedic Institute of Western KY
mi
from
Paducah, KY
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