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
13,253
archived clinical trials in
Arthritis

A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Albuquerque, NM
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Albuquerque, NM
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Hartsdale, NY
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Hartsdale, NY
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Rochester, NY
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Rochester, NY
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Charlotte, NC
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Charlotte, NC
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Raleigh, NC
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Raleigh, NC
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Duncansville, PA
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Duncansville, PA
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Mount Pleasant, SC
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Mount Pleasant, SC
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Franklin, TN
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Franklin, TN
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Austin, TX
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Austin, TX
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Baytown, TX
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Baytown, TX
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Desoto, TX
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Desoto, TX
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Wichita Falls, TX
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Wichita Falls, TX
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Newport News, VA
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Newport News, VA
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Bellevue, WA
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Bellevue, WA
Click here to add this to my saved trials
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated:  12/31/1969
mi
from
Broadmeadow,
A Study to Assess the Efficacy and Safety of AXS-02 in Subjects With Knee OA Associated With Bone Marrow Lesions
COAST -1: Clinical Knee Osteoarthritis Symptom Treatment 1 Study. A Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered Orally to Subjects With Knee Osteoarthritis Associated With Bone Marrow Lesions.
Status: Enrolling
Updated: 12/31/1969
mi
from
Broadmeadow,
Click here to add this to my saved trials
Quality IQ Patient Simulation Physician Practice Measurement and Engagement
Quality IQ Patient Simulation Physician Practice Measurement and Engagement
Status: Enrolling
Updated:  12/31/1969
QURE Healthcare
mi
from
San Francisco, CA
Quality IQ Patient Simulation Physician Practice Measurement and Engagement
Quality IQ Patient Simulation Physician Practice Measurement and Engagement
Status: Enrolling
Updated: 12/31/1969
QURE Healthcare
mi
from
San Francisco, CA
Click here to add this to my saved trials
A Fish Oil Supplement to Maintain Body Weight in Patients With Disease-Related Weight Loss
AAFA™ Fish Oil Nutritional Supplementation to Maintain Body Weight in Patients With Disease-Related Weight Loss
Status: Enrolling
Updated:  12/31/1969
Johns Hopkins Hospital
mi
from
Baltimore, MD
A Fish Oil Supplement to Maintain Body Weight in Patients With Disease-Related Weight Loss
AAFA™ Fish Oil Nutritional Supplementation to Maintain Body Weight in Patients With Disease-Related Weight Loss
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Hospital
mi
from
Baltimore, MD
Click here to add this to my saved trials
Clinical Evaluation of the TITAN™ Total Shoulder System
A Post-Market Observational Study to Evaluate Performance and Safety of the TITAN™ Total Shoulder System
Status: Enrolling
Updated:  12/31/1969
OrthoIndy
mi
from
Indianapolis, IN
Clinical Evaluation of the TITAN™ Total Shoulder System
A Post-Market Observational Study to Evaluate Performance and Safety of the TITAN™ Total Shoulder System
Status: Enrolling
Updated: 12/31/1969
OrthoIndy
mi
from
Indianapolis, IN
Click here to add this to my saved trials
Clinical Evaluation of the TITAN™ Total Shoulder System
A Post-Market Observational Study to Evaluate Performance and Safety of the TITAN™ Total Shoulder System
Status: Enrolling
Updated:  12/31/1969
Rothman Institute
mi
from
Philadelphia, PA
Clinical Evaluation of the TITAN™ Total Shoulder System
A Post-Market Observational Study to Evaluate Performance and Safety of the TITAN™ Total Shoulder System
Status: Enrolling
Updated: 12/31/1969
Rothman Institute
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Parabens Flocculation on the Anti Inflammatory Effects of Corticosteroid Injections for Total Knee Arthroplasty
Clinical Significance of Parabens Flocculation on the Anti Inflrammmatory Effects of Corticosteroid Injection Osteoarthritic Knees
Status: Enrolling
Updated:  12/31/1969
Loma Linda University Health, Department of Orthopaedic Surgery
mi
from
Loma Linda, CA
Parabens Flocculation on the Anti Inflammatory Effects of Corticosteroid Injections for Total Knee Arthroplasty
Clinical Significance of Parabens Flocculation on the Anti Inflrammmatory Effects of Corticosteroid Injection Osteoarthritic Knees
Status: Enrolling
Updated: 12/31/1969
Loma Linda University Health, Department of Orthopaedic Surgery
mi
from
Loma Linda, CA
Click here to add this to my saved trials
Total Hip Arthroplasty Outcomes With Regional and Multimodal Analgesia
Improvement in Total Hip Arthroplasty Patient Outcomes With Regional Anesthesia and Multimodal Analgesia: A Retrospective Analysis
Status: Enrolling
Updated:  12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
Total Hip Arthroplasty Outcomes With Regional and Multimodal Analgesia
Improvement in Total Hip Arthroplasty Patient Outcomes With Regional Anesthesia and Multimodal Analgesia: A Retrospective Analysis
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
Click here to add this to my saved trials
Biofreeze® vs. a Placebo on Knee Osteoarthritis Walking Gait Characteristics and Pain
The Effect of Biofreeze® vs. a Placebo on Knee Osteoarthritis Walking Gait Characteristics and Pain
Status: Enrolling
Updated:  12/31/1969
Sport & Spine Rehab
mi
from
Rockville, MD
Biofreeze® vs. a Placebo on Knee Osteoarthritis Walking Gait Characteristics and Pain
The Effect of Biofreeze® vs. a Placebo on Knee Osteoarthritis Walking Gait Characteristics and Pain
Status: Enrolling
Updated: 12/31/1969
Sport & Spine Rehab
mi
from
Rockville, MD
Click here to add this to my saved trials
Closed Suction Drainage in Shoulder Arthroplasty
The Utility of Closed Suction Drainage in Total Shoulder Arthroplasty: A Prospective Analysis.
Status: Enrolling
Updated:  12/31/1969
Columbia University Medical Center
mi
from
New York, NY
Closed Suction Drainage in Shoulder Arthroplasty
The Utility of Closed Suction Drainage in Total Shoulder Arthroplasty: A Prospective Analysis.
Status: Enrolling
Updated: 12/31/1969
Columbia University Medical Center
mi
from
New York, NY
Click here to add this to my saved trials
Efficacy of Celecoxib Vs Placebo to Prevent Pain in a Paced Walk
A Double-Blind, Placebo-Controlled, Crossover Pilot Study of the Efficacy of Celecoxib 200 Mg Qd in Relieving Pain and Walking Dysfunction in Osteoarthritis of the Knee
Status: Enrolling
Updated:  9/13/2005
University Hospitals of Cleveland
mi
from
Cleveland, OH
Efficacy of Celecoxib Vs Placebo to Prevent Pain in a Paced Walk
A Double-Blind, Placebo-Controlled, Crossover Pilot Study of the Efficacy of Celecoxib 200 Mg Qd in Relieving Pain and Walking Dysfunction in Osteoarthritis of the Knee
Status: Enrolling
Updated: 9/13/2005
University Hospitals of Cleveland
mi
from
Cleveland, OH
Click here to add this to my saved trials
Intra-articularInjection of Botulinum Toxin Type
Intra-articularInjection of Botulinum Toxin Type a for the Treatment of Chronic Knee Pain: A Randomized, Placebo Controlled, Double Blind Study
Status: Enrolling
Updated:  9/13/2005
Minneapolis VAMC
mi
from
Minneapolis, MN
Intra-articularInjection of Botulinum Toxin Type
Intra-articularInjection of Botulinum Toxin Type a for the Treatment of Chronic Knee Pain: A Randomized, Placebo Controlled, Double Blind Study
Status: Enrolling
Updated: 9/13/2005
Minneapolis VAMC
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Intra-Articular Injection of Botulinum Toxin Type A for Shoulder Pain
Intra-Articular Injection of Botulinum Toxin Type A for the Treatment of Shoulder Pain: A Randomized, Double Blinded, Placebo Controlled Trial
Status: Enrolling
Updated:  11/2/2005
Minneapolis VAMC
mi
from
Minneapolis, MN
Intra-Articular Injection of Botulinum Toxin Type A for Shoulder Pain
Intra-Articular Injection of Botulinum Toxin Type A for the Treatment of Shoulder Pain: A Randomized, Double Blinded, Placebo Controlled Trial
Status: Enrolling
Updated: 11/2/2005
Minneapolis VAMC
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Study of the Use of Laser Light to Treat Osteoarthritis of the Hand.
Ultra Probe Laser System Osteoarthritis of the Hand Clinical Study.
Status: Enrolling
Updated:  11/14/2005
Proctology Associates
mi
from
Phoenix, AZ
Study of the Use of Laser Light to Treat Osteoarthritis of the Hand.
Ultra Probe Laser System Osteoarthritis of the Hand Clinical Study.
Status: Enrolling
Updated: 11/14/2005
Proctology Associates
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Study of the Use of Laser Light to Treat Osteoarthritis of the Hand.
Ultra Probe Laser System Osteoarthritis of the Hand Clinical Study.
Status: Enrolling
Updated:  11/14/2005
Advanced Wellness Center
mi
from
Long Beach, CA
Study of the Use of Laser Light to Treat Osteoarthritis of the Hand.
Ultra Probe Laser System Osteoarthritis of the Hand Clinical Study.
Status: Enrolling
Updated: 11/14/2005
Advanced Wellness Center
mi
from
Long Beach, CA
Click here to add this to my saved trials
Study of the Use of Laser Light to Treat Osteoarthritis of the Hand.
Ultra Probe Laser System Osteoarthritis of the Hand Clinical Study.
Status: Enrolling
Updated:  11/14/2005
Advanced Chiropractic
mi
from
Bloomington, MN
Study of the Use of Laser Light to Treat Osteoarthritis of the Hand.
Ultra Probe Laser System Osteoarthritis of the Hand Clinical Study.
Status: Enrolling
Updated: 11/14/2005
Advanced Chiropractic
mi
from
Bloomington, MN
Click here to add this to my saved trials
Do Corticosteroid Injections During Total Knee Replacement Improve Early Clinical Results?
Peri-Articular Injections Containing a Corticosteroid During Total Knee Arthroplasty
Status: Enrolling
Updated:  6/25/2007
Lexington Clinic Sports Medicine Center
mi
from
Lexington, KY
Do Corticosteroid Injections During Total Knee Replacement Improve Early Clinical Results?
Peri-Articular Injections Containing a Corticosteroid During Total Knee Arthroplasty
Status: Enrolling
Updated: 6/25/2007
Lexington Clinic Sports Medicine Center
mi
from
Lexington, KY
Click here to add this to my saved trials
Postoperative Function Following Partial and Total Knee Replacement
Postoperative Function Following Partial and Total Knee Replacement
Status: Enrolling
Updated:  6/26/2007
Lexington Clinic Sports Medicine Center
mi
from
Lexington, KY
Postoperative Function Following Partial and Total Knee Replacement
Postoperative Function Following Partial and Total Knee Replacement
Status: Enrolling
Updated: 6/26/2007
Lexington Clinic Sports Medicine Center
mi
from
Lexington, KY
Click here to add this to my saved trials
The Role of Intra-Operative Intracapsular Blocks in Post-Operative Pain Management Following Total Knee Arthroplasty
The Role of Intra-Operative Intracapsular Blocks in Post-Operative Pain Management Following Total Knee Arthroplasty: A Double-Blinded Randomized Controlled Trial
Status: Enrolling
Updated:  2/27/2008
Duke University Adult Reconstructive Surgery
mi
from
Durham, NC
The Role of Intra-Operative Intracapsular Blocks in Post-Operative Pain Management Following Total Knee Arthroplasty
The Role of Intra-Operative Intracapsular Blocks in Post-Operative Pain Management Following Total Knee Arthroplasty: A Double-Blinded Randomized Controlled Trial
Status: Enrolling
Updated: 2/27/2008
Duke University Adult Reconstructive Surgery
mi
from
Durham, NC
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Dose Escalation Study Of Chinese Herbs In Osteoarthritis Of The Knee
Dose Escalation Study Of Chinese Herbs In Osteoarthritis Of The Knee
Status: Enrolling
Updated:  9/17/2008
University of Maryland Center for Integrative Medicine Kernan Hospital
mi
from
Baltimore, MD
Dose Escalation Study Of Chinese Herbs In Osteoarthritis Of The Knee
Dose Escalation Study Of Chinese Herbs In Osteoarthritis Of The Knee
Status: Enrolling
Updated: 9/17/2008
University of Maryland Center for Integrative Medicine Kernan Hospital
mi
from
Baltimore, MD
Click here to add this to my saved trials
Osteoarthritis Bedside Testing Kit
Development of a Bedside Pain Assessment Kit for Evaluating Effectiveness of Drugs for Osteoarthritis
Status: Enrolling
Updated:  11/19/2008
Analgesic Research, LLC
mi
from
Needham, MA
Osteoarthritis Bedside Testing Kit
Development of a Bedside Pain Assessment Kit for Evaluating Effectiveness of Drugs for Osteoarthritis
Status: Enrolling
Updated: 11/19/2008
Analgesic Research, LLC
mi
from
Needham, MA
Click here to add this to my saved trials
An Open Label Trial for Treating Carpometacarpal Osteoarthritis of the Thumb: Pilot Study
An Open Label Trial for Treating Carpometacarpal Osteoarthritis: A Pilot Study Sub Study: Validation of the Strength-Dexterity Test in Subjects Without Carpometacarpal Osteoarthritis
Status: Enrolling
Updated:  1/27/2009
Hospital for Special Surgery
mi
from
New York, NY
An Open Label Trial for Treating Carpometacarpal Osteoarthritis of the Thumb: Pilot Study
An Open Label Trial for Treating Carpometacarpal Osteoarthritis: A Pilot Study Sub Study: Validation of the Strength-Dexterity Test in Subjects Without Carpometacarpal Osteoarthritis
Status: Enrolling
Updated: 1/27/2009
Hospital for Special Surgery
mi
from
New York, NY
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Restoration of Leg Length, Offset, and Center of Rotation in Total Hip Replacement
Restoration of Leg Length, Offset, and Center of Rotation in Total Hip Replacement
Status: Enrolling
Updated:  2/5/2009
Baptist Hospital
mi
from
Nashville, TN
Restoration of Leg Length, Offset, and Center of Rotation in Total Hip Replacement
Restoration of Leg Length, Offset, and Center of Rotation in Total Hip Replacement
Status: Enrolling
Updated: 2/5/2009
Baptist Hospital
mi
from
Nashville, TN
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A Study Evaluating the Safety and Efficacy of Cura-100 in Subjects With Rheumatoid Arthritis and Osteoarthritis
Study Evaluating Cura-100 in Rheumatoid Arthritis and Osteoarthritis
Status: Enrolling
Updated:  2/18/2009
Cura Biotech LLC
mi
from
Sunnyvale, CA
A Study Evaluating the Safety and Efficacy of Cura-100 in Subjects With Rheumatoid Arthritis and Osteoarthritis
Study Evaluating Cura-100 in Rheumatoid Arthritis and Osteoarthritis
Status: Enrolling
Updated: 2/18/2009
Cura Biotech LLC
mi
from
Sunnyvale, CA
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Mobile, AL
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Mobile, AL
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Montgomery, AL
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Montgomery, AL
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Tuscaloosa, AL
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Tuscaloosa, AL
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Chandler, AZ
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Chandler, AZ
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Mesa, AZ
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Mesa, AZ
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Phoenix, AZ
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Phoenix, AZ
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Fair Oaks, CA
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Fair Oaks, CA
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
San Diego, CA
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
San Diego, CA
Click here to add this to my saved trials
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Santa Barbara, CA
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Santa Barbara, CA
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Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Northglenn, CO
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Northglenn, CO
Click here to add this to my saved trials
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Coral Gables, FL
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Coral Gables, FL
Click here to add this to my saved trials
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated:  2/19/2009
Clinical Research Facility
mi
from
Daytona Beach, FL
Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Hip
A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo Bid and Naproxen 500 mg Bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HCT3012) 750 mg Bid, in Patients With Osteoarthritis of the Hip
Status: Enrolling
Updated: 2/19/2009
Clinical Research Facility
mi
from
Daytona Beach, FL
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