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

CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Dallas, TX
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Dallas, TX
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
San Antonio, TX
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
San Antonio, TX
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Bellevue, WA
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Bellevue, WA
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Seattle, WA
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Seattle, WA
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Madison, WI
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Madison, WI
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
mi
from
Broadmeadow,
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
mi
from
Broadmeadow,
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Tucson, AZ
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Tucson, AZ
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Encinitas, CA
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Encinitas, CA
Click here to add this to my saved trials
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated:  3/21/2018
Clinical Research Facility
mi
from
Denver, CO
CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1
CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)
Status: Enrolling
Updated: 3/21/2018
Clinical Research Facility
mi
from
Denver, CO
Click here to add this to my saved trials
Clinical Neuropharmacology of Pain in Spinal Cord Injury- Dextromethorphan/Lidocaine Combination Clinical Trial
Clinical Neuropharmacology of Pain in Spinal Cord Injury- Dextromethorphan/Lidocaine Combination (Factorial Design) Clinical Trial
Status: Enrolling
Updated:  3/21/2018
Translational Pain Research, Brigham and Women's Hospital
mi
from
Boston, MA
Clinical Neuropharmacology of Pain in Spinal Cord Injury- Dextromethorphan/Lidocaine Combination Clinical Trial
Clinical Neuropharmacology of Pain in Spinal Cord Injury- Dextromethorphan/Lidocaine Combination (Factorial Design) Clinical Trial
Status: Enrolling
Updated: 3/21/2018
Translational Pain Research, Brigham and Women's Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
Effect of Deep Brain Stimulation (DBS) on Sleep Architecture in Patients With Movement Disorders
Effect of DBS on Sleep Architecture in Patients With Movement Disorders.
Status: Enrolling
Updated:  3/22/2018
University of Alabama at Birmingham
mi
from
Birmingham, AL
Effect of Deep Brain Stimulation (DBS) on Sleep Architecture in Patients With Movement Disorders
Effect of DBS on Sleep Architecture in Patients With Movement Disorders.
Status: Enrolling
Updated: 3/22/2018
University of Alabama at Birmingham
mi
from
Birmingham, AL
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Alabama Clinical Therapeutics, Llc
mi
from
Birmingham, AL
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Alabama Clinical Therapeutics, Llc
mi
from
Birmingham, AL
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
HOPE Research Institute
mi
from
Phoenix, AZ
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
HOPE Research Institute
mi
from
Phoenix, AZ
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Arizona Pain Specialists
mi
from
Scottsdale, AZ
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Arizona Pain Specialists
mi
from
Scottsdale, AZ
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Medhat Mikhael, M.D. Inc.
mi
from
Fountain Valley, CA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Medhat Mikhael, M.D. Inc.
mi
from
Fountain Valley, CA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Orthopedic Pain Specialists
mi
from
Santa Monica, CA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Orthopedic Pain Specialists
mi
from
Santa Monica, CA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Integrated Pain Management Medical Group, Inc.
mi
from
Walnut Creek, CA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Integrated Pain Management Medical Group, Inc.
mi
from
Walnut Creek, CA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Holy Cross Hospital
mi
from
Fort Lauderdale, FL
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Holy Cross Hospital
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Florida Pain Institute
mi
from
Merritt Island, FL
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Florida Pain Institute
mi
from
Merritt Island, FL
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Pain Care LLC
mi
from
Stockbridge, GA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Pain Care LLC
mi
from
Stockbridge, GA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
American Health Network Of In Llc
mi
from
Muncie, IN
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
American Health Network Of In Llc
mi
from
Muncie, IN
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Pain Management Associates
mi
from
Independence, MO
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Pain Management Associates
mi
from
Independence, MO
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
University Pain Medicine Center
mi
from
Somerset, NJ
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
University Pain Medicine Center
mi
from
Somerset, NJ
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Oklahoma Pain Physicians
mi
from
Oklahoma City, OK
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Oklahoma Pain Physicians
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Performance Spine and Sports Physicians
mi
from
Pottstown, PA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Performance Spine and Sports Physicians
mi
from
Pottstown, PA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
SC Pain & Spine Specialists
mi
from
Murrells Inlet, SC
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
SC Pain & Spine Specialists
mi
from
Murrells Inlet, SC
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Spine Team Texas
mi
from
Southlake, TX
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Spine Team Texas
mi
from
Southlake, TX
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Virginia iSpine Physicians
mi
from
Richmond, VA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Virginia iSpine Physicians
mi
from
Richmond, VA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
Penn State Hershey Medical Center
mi
from
Hershey, PA
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
Penn State Hershey Medical Center
mi
from
Hershey, PA
Click here to add this to my saved trials
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated:  3/28/2018
GWU - Medical Faculty Associates, Inc.
mi
from
Washington,
The STEPS - Totalis™ Trial
A Prospective, Multi-center, Randomized Controlled Double-Blind Trial Evaluating the VertiFlex® Totalis™ Direct Decompression System Versus a Sham Surgical Procedure in Patients With Lumbar Spinal Stenosis
Status: Enrolling
Updated: 3/28/2018
GWU - Medical Faculty Associates, Inc.
mi
from
Washington,
Click here to add this to my saved trials
Efficacy Study of Femoral Nerve Block in Children With a Femur Fracture
Examining the Efficacy of Femoral Nerve Block in Children With a Femoral Shaft Fracture
Status: Enrolling
Updated:  3/28/2018
St. Louis Children's Hospital
mi
from
Saint Louis, MO
Efficacy Study of Femoral Nerve Block in Children With a Femur Fracture
Examining the Efficacy of Femoral Nerve Block in Children With a Femoral Shaft Fracture
Status: Enrolling
Updated: 3/28/2018
St. Louis Children's Hospital
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Efficacy Study of Femoral Nerve Block in Children With a Femur Fracture
Examining the Efficacy of Femoral Nerve Block in Children With a Femoral Shaft Fracture
Status: Enrolling
Updated:  3/28/2018
Washington University
mi
from
Saint Louis, MO
Efficacy Study of Femoral Nerve Block in Children With a Femur Fracture
Examining the Efficacy of Femoral Nerve Block in Children With a Femoral Shaft Fracture
Status: Enrolling
Updated: 3/28/2018
Washington University
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Enhance Wellness for Individuals With Long-Term Physical Disabilities
Project Enhance for Adults Aging With Long-Term Physical Disability
Status: Enrolling
Updated:  3/30/2018
Univ of Washington
mi
from
Seattle, WA
Enhance Wellness for Individuals With Long-Term Physical Disabilities
Project Enhance for Adults Aging With Long-Term Physical Disability
Status: Enrolling
Updated: 3/30/2018
Univ of Washington
mi
from
Seattle, WA
Click here to add this to my saved trials
Tacrolimus, Bortezomib, & Thymoglobulin in Preventing Low Toxicity GVHD in Donor Blood Stem Cell Transplant Patients
Phase II Trial of Low Toxicity GVHD Prevention and Enhanced Immune Recovery With Tacrolimus, Bortezomib and Thymoglobulin® TBT
Status: Enrolling
Updated:  3/30/2018
Emory University/Winship Cancer Institute
mi
from
Atlanta, GA
Tacrolimus, Bortezomib, & Thymoglobulin in Preventing Low Toxicity GVHD in Donor Blood Stem Cell Transplant Patients
Phase II Trial of Low Toxicity GVHD Prevention and Enhanced Immune Recovery With Tacrolimus, Bortezomib and Thymoglobulin® TBT
Status: Enrolling
Updated: 3/30/2018
Emory University/Winship Cancer Institute
mi
from
Atlanta, GA
Click here to add this to my saved trials
Comparing Functional Outcomes in Individuals Using Micro-processor Controlled Orthosis Versus Stance Control Orthosis
Micro-processor Controlled Knee-Ankle-Foot Orthosis (C-Brace) Versus Stance-control Knee-Ankle-Foot Orthosis (SCO): Functional Outcomes in Individuals With Lower Extremity Impairment
Status: Enrolling
Updated:  4/3/2018
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Comparing Functional Outcomes in Individuals Using Micro-processor Controlled Orthosis Versus Stance Control Orthosis
Micro-processor Controlled Knee-Ankle-Foot Orthosis (C-Brace) Versus Stance-control Knee-Ankle-Foot Orthosis (SCO): Functional Outcomes in Individuals With Lower Extremity Impairment
Status: Enrolling
Updated: 4/3/2018
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Click here to add this to my saved trials
Identify Training Strategies for Progressing Exoskeleton Users Towards Everyday Functional Ambulation
Identify Training Strategies for Progressing Exoskeleton Users Towards Everyday Functional Ambulation
Status: Enrolling
Updated:  4/3/2018
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Identify Training Strategies for Progressing Exoskeleton Users Towards Everyday Functional Ambulation
Identify Training Strategies for Progressing Exoskeleton Users Towards Everyday Functional Ambulation
Status: Enrolling
Updated: 4/3/2018
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
The Orthopaedic Center; Crestwood Medical Center
mi
from
Huntsville, AL
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
The Orthopaedic Center; Crestwood Medical Center
mi
from
Huntsville, AL
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Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Todd Lanman, MD, FACS, A Professional Corp.;
mi
from
Beverly Hills, CA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Todd Lanman, MD, FACS, A Professional Corp.;
mi
from
Beverly Hills, CA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Bone & Spine Surgery
mi
from
Colton, CA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Bone & Spine Surgery
mi
from
Colton, CA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
La Jolla Neurological Associates, AMC; Scripps Memorial Hospital La Jolla; Scripps Memorial Hospital Encinitas
mi
from
La Jolla, CA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
La Jolla Neurological Associates, AMC; Scripps Memorial Hospital La Jolla; Scripps Memorial Hospital Encinitas
mi
from
La Jolla, CA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
St. Mary's Spine Center; St. Mary's Hospital
mi
from
San Francisco, CA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
St. Mary's Spine Center; St. Mary's Hospital
mi
from
San Francisco, CA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Delaware Neurosurgical Group; Christiana Care Health Systems
mi
from
Newark, DE
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Delaware Neurosurgical Group; Christiana Care Health Systems
mi
from
Newark, DE
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Spinal Associates, Gulf Coast Hospital
mi
from
Panama City, FL
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Spinal Associates, Gulf Coast Hospital
mi
from
Panama City, FL
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Peachtree Neurosurgery, Northside Hospital
mi
from
Atlanta, GA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Peachtree Neurosurgery, Northside Hospital
mi
from
Atlanta, GA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
The Hughston Clinic, P.C., Hughston Hospital and Rehabilitation Center
mi
from
Columbus, GA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
The Hughston Clinic, P.C., Hughston Hospital and Rehabilitation Center
mi
from
Columbus, GA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Neuro Spine & Pain Center; Lutheran Hospital
mi
from
Fort Wayne, IN
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Neuro Spine & Pain Center; Lutheran Hospital
mi
from
Fort Wayne, IN
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Great Lakes Neurosurgical; Spectrum Health East Campus
mi
from
Grand Rapids, MI
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Great Lakes Neurosurgical; Spectrum Health East Campus
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Adams Neurosurgery; Mid Michigan Medical Center
mi
from
Saginaw, MI
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Adams Neurosurgery; Mid Michigan Medical Center
mi
from
Saginaw, MI
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
The Orthopedic Center of St. Louis; Barnes Jewish West County Hospital
mi
from
Chesterfield, MO
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
The Orthopedic Center of St. Louis; Barnes Jewish West County Hospital
mi
from
Chesterfield, MO
Click here to add this to my saved trials