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
33,560
archived clinical trials in
Neurology

A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of Pittsburgh Cancer Institute
mi
from
Pittsburgh, PA
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of Pittsburgh Cancer Institute
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
York Hospital
mi
from
York, PA
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
York Hospital
mi
from
York, PA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Medical University of South Carolina; MSC 300
mi
from
Charleston, SC
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina; MSC 300
mi
from
Charleston, SC
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of South Carolina School of Medicine
mi
from
Columbia, SC
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of South Carolina School of Medicine
mi
from
Columbia, SC
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Neurology and Pain Clinic, LLC
mi
from
Orangeburg, SC
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Neurology and Pain Clinic, LLC
mi
from
Orangeburg, SC
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Chattanooga Center for Neurologic Research
mi
from
Chattanooga, TN
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Chattanooga Center for Neurologic Research
mi
from
Chattanooga, TN
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of Tennessee Medical Center
mi
from
Knoxville, TN
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of Tennessee Medical Center
mi
from
Knoxville, TN
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Valley Baptist Medical Center
mi
from
Harlingen, TX
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Valley Baptist Medical Center
mi
from
Harlingen, TX
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Methodist Neurological Institute
mi
from
Houston, TX
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Methodist Neurological Institute
mi
from
Houston, TX
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of Texas Health Science Center at Houston
mi
from
Houston, TX
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of Texas Health Science Center at Houston
mi
from
Houston, TX
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Texas Tech Univ. Hlth Sci. Ctr.
mi
from
Lubbock, TX
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Texas Tech Univ. Hlth Sci. Ctr.
mi
from
Lubbock, TX
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University Hospital - San Antonio
mi
from
San Antonio, TX
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University Hospital - San Antonio
mi
from
San Antonio, TX
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of Utah
mi
from
Salt Lake City, UT
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of Utah
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Inova Fairfax Hospital
mi
from
Fairfax, VA
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Inova Fairfax Hospital
mi
from
Fairfax, VA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Swedish Medical Center
mi
from
Seattle, WA
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Swedish Medical Center
mi
from
Seattle, WA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
West Virginia University Hospital
mi
from
Morgantown, WV
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
West Virginia University Hospital
mi
from
Morgantown, WV
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
Gunderson Health System
mi
from
La Crosse, WI
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
Gunderson Health System
mi
from
La Crosse, WI
Click here to add this to my saved trials
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated:  12/31/1969
University of Wisconsin
mi
from
Madison, WI
A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke
A Phase IIIB, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Alteplase in Patients With Mild Stroke: Rapidly Improving Symptoms and Minor Neurologic Deficits (PRISMS)
Status: Enrolling
Updated: 12/31/1969
University of Wisconsin
mi
from
Madison, WI
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
San Diego, CA
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
San Diego, CA
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Englewood, CO
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Englewood, CO
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Gainesville, FL
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Gainesville, FL
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Tampa, FL
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Tampa, FL
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Baltimore, MD
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Baltimore, MD
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
New York, NY
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
New York, NY
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Memphis, TN
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Memphis, TN
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Houston, TX
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Houston, TX
Click here to add this to my saved trials
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Kirkland, WA
Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Kirkland, WA
Click here to add this to my saved trials
Heart-Brain Retraining for Stroke Rehabilitation
Heart-Brain Retraining: Forced Aerobic Exercise for Stroke Rehabilitation
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
Heart-Brain Retraining for Stroke Rehabilitation
Heart-Brain Retraining: Forced Aerobic Exercise for Stroke Rehabilitation
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Desert Institute for Spine Care
mi
from
Phoenix, AZ
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Desert Institute for Spine Care
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Todd Lanman, MD, FACS
mi
from
Beverly Hills, CA
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Todd Lanman, MD, FACS
mi
from
Beverly Hills, CA
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Stanford University Hospital
mi
from
Palo Alto, CA
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Stanford University Hospital
mi
from
Palo Alto, CA
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Rocky Mountain Associates in Orthopedic Medicine
mi
from
Johnstown, CO
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Rocky Mountain Associates in Orthopedic Medicine
mi
from
Johnstown, CO
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Midwest Orthopaedics at Rush
mi
from
Chicago, IL
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Midwest Orthopaedics at Rush
mi
from
Chicago, IL
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Indiana Spine Group
mi
from
Carmel, IN
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Indiana Spine Group
mi
from
Carmel, IN
Click here to add this to my saved trials
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Greater Baltimore Neurological Associates
mi
from
Baltimore, MD
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Greater Baltimore Neurological Associates
mi
from
Baltimore, MD
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Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Hospital for Special Surgery
mi
from
New York, NY
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Hospital for Special Surgery
mi
from
New York, NY
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Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Carolina NeuroSurgery & Spine Associates
mi
from
Charlotte, NC
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Carolina NeuroSurgery & Spine Associates
mi
from
Charlotte, NC
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Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Triangle Orthopedic Associates, P.A.
mi
from
Durham, NC
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Triangle Orthopedic Associates, P.A.
mi
from
Durham, NC
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Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Center for Sports Medicine and Orthopaedics
mi
from
Chattanooga, TN
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Center for Sports Medicine and Orthopaedics
mi
from
Chattanooga, TN
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Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Lakeway Regional Medical Center
mi
from
Lakeway, TX
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Lakeway Regional Medical Center
mi
from
Lakeway, TX
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Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated:  12/31/1969
Texas Back Institute
mi
from
Plano, TX
Restore CLINICAL TRIAL
Prospective, Non-Randomized, Concurrently Controlled, Multi-Center Study to Evaluate the Safety and Effectiveness of the Spinal Kinetics™ M6-C Artificial Cervical Disc Compared to Anterior Cervical Discectomy and Fusion (ACDF) for the Treatment of Symptomatic Cervical Radiculopathy
Status: Enrolling
Updated: 12/31/1969
Texas Back Institute
mi
from
Plano, TX
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Long-term Surveillance of the MedStream Programmable Infusion System
Long-term Surveillance of the MedStream Programmable Infusion System for the Intrathecal Infusion of Baclofen in the Treatment of Spasticity
Status: Enrolling
Updated:  12/31/1969
The Methodist Hospital Research Institute
mi
from
Houston, TX
Long-term Surveillance of the MedStream Programmable Infusion System
Long-term Surveillance of the MedStream Programmable Infusion System for the Intrathecal Infusion of Baclofen in the Treatment of Spasticity
Status: Enrolling
Updated: 12/31/1969
The Methodist Hospital Research Institute
mi
from
Houston, TX
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Long-term Surveillance of the MedStream Programmable Infusion System
Long-term Surveillance of the MedStream Programmable Infusion System for the Intrathecal Infusion of Baclofen in the Treatment of Spasticity
Status: Enrolling
Updated:  12/31/1969
UMASS Memorial Medical Center
mi
from
Worcester, MA
Long-term Surveillance of the MedStream Programmable Infusion System
Long-term Surveillance of the MedStream Programmable Infusion System for the Intrathecal Infusion of Baclofen in the Treatment of Spasticity
Status: Enrolling
Updated: 12/31/1969
UMASS Memorial Medical Center
mi
from
Worcester, MA
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Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Status: Enrolling
Updated:  12/31/1969
Boston Children's Hospital, 300 Longwood Avenue
mi
from
Boston, MA
Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Status: Enrolling
Updated: 12/31/1969
Boston Children's Hospital, 300 Longwood Avenue
mi
from
Boston, MA
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Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Status: Enrolling
Updated:  12/31/1969
Centre Hospitalier Regional de la Citadelle
mi
from
Liège,
Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Status: Enrolling
Updated: 12/31/1969
Centre Hospitalier Regional de la Citadelle
mi
from
Liège,
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Therapeutic Resources for Attention Improvement With Neuroimaging for TBI
Therapeutic Resources for Attention Improvement With Neuroimaging for Traumatic Brain Injury
Status: Enrolling
Updated:  12/31/1969
UCSF Mission Bay
mi
from
San Francisco, CA
Therapeutic Resources for Attention Improvement With Neuroimaging for TBI
Therapeutic Resources for Attention Improvement With Neuroimaging for Traumatic Brain Injury
Status: Enrolling
Updated: 12/31/1969
UCSF Mission Bay
mi
from
San Francisco, CA
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Effect of Milk Oligosaccharides and Bifidobacteria on the Intestinal Microflora of Children With Autism
A Pilot Study Examining Microbiota Composition in Children With Autism and Gastrointestinal Symptoms After Use of Bifidobacterium Infantis and Milk Oligosaccharides
Status: Enrolling
Updated:  12/31/1969
UC Davis MIND Institute
mi
from
Sacramento, CA
Effect of Milk Oligosaccharides and Bifidobacteria on the Intestinal Microflora of Children With Autism
A Pilot Study Examining Microbiota Composition in Children With Autism and Gastrointestinal Symptoms After Use of Bifidobacterium Infantis and Milk Oligosaccharides
Status: Enrolling
Updated: 12/31/1969
UC Davis MIND Institute
mi
from
Sacramento, CA
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The Effects of ProFoveate on Reducing Self-Stimulating Behaviors
The Effects of ProFoveate on Reducing Self-Stimulating Behaviors in Children Diagnosed With Autism Spectrum Disorders
Status: Enrolling
Updated:  12/31/1969
University of Arkansas at Little Rock Speech and Hearing Clinic
mi
from
Little Rock, AR
The Effects of ProFoveate on Reducing Self-Stimulating Behaviors
The Effects of ProFoveate on Reducing Self-Stimulating Behaviors in Children Diagnosed With Autism Spectrum Disorders
Status: Enrolling
Updated: 12/31/1969
University of Arkansas at Little Rock Speech and Hearing Clinic
mi
from
Little Rock, AR
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Mayo Clinic Traumatic Brain Injury Model System Center: The CONNECT Trial
The CONNECT Trial: A Randomized Pragmatic Clinical Trial Measuring the Effectiveness of a Remotely Provided Complex Brain Rehabilitation Intervention in Improving Participation Outcomes of Individuals With TBI, Their Families, and Local Primary Providers
Status: Enrolling
Updated:  12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
Mayo Clinic Traumatic Brain Injury Model System Center: The CONNECT Trial
The CONNECT Trial: A Randomized Pragmatic Clinical Trial Measuring the Effectiveness of a Remotely Provided Complex Brain Rehabilitation Intervention in Improving Participation Outcomes of Individuals With TBI, Their Families, and Local Primary Providers
Status: Enrolling
Updated: 12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
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