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
17,797
archived clinical trials in
Peripheral Vascular Disease

Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Dartmouth Hitchcock Medical Center
mi
from
Lebanon, NH
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Dartmouth Hitchcock Medical Center
mi
from
Lebanon, NH
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Holy Name Medical Center
mi
from
Teaneck, NJ
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Holy Name Medical Center
mi
from
Teaneck, NJ
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
New York Presbyterian Hospital - Columbia University Medical Center
mi
from
New York, NY
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
New York Presbyterian Hospital - Columbia University Medical Center
mi
from
New York, NY
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Wake Forest Baptist Health
mi
from
Winston-Salem, NC
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Wake Forest Baptist Health
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
University of Oklahoma - Physicians Surgical Specialists
mi
from
Tulsa, OK
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
University of Oklahoma - Physicians Surgical Specialists
mi
from
Tulsa, OK
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Oregon Health and Science University
mi
from
Portland, OR
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Oregon Health and Science University
mi
from
Portland, OR
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Veterans Affairs Medical Center
mi
from
Pittsburgh, PA
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Veterans Affairs Medical Center
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Medical University of South Carolina
mi
from
Charleston, SC
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Medical University of South Carolina
mi
from
Charleston, SC
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Sanford Health
mi
from
Sioux Falls, SD
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Sanford Health
mi
from
Sioux Falls, SD
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
The Methodist Hospital Research Institute
mi
from
Houston, TX
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
The Methodist Hospital Research Institute
mi
from
Houston, TX
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Antwerpen University Hospital
mi
from
Edegem,
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Antwerpen University Hospital
mi
from
Edegem,
Click here to add this to my saved trials
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated:  4/24/2017
Mercy Hospital, St. Louis
mi
from
Saint Louis, MO
Efficacy and Safety of AMG0001 in Subjects With Critical Limb Ischemia
A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AMG0001 in Subjects With Critical Limb Ischemia
Status: Enrolling
Updated: 4/24/2017
Mercy Hospital, St. Louis
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Controlled Joint Disease
Adalimumab to Mitigate Cardiovascular Risk in RA Patients With Well-Controlled Joint Disease
Status: Enrolling
Updated:  5/1/2017
University of California, San Francisco, San Francisco General Hospital
mi
from
San Francisco, CA
Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Controlled Joint Disease
Adalimumab to Mitigate Cardiovascular Risk in RA Patients With Well-Controlled Joint Disease
Status: Enrolling
Updated: 5/1/2017
University of California, San Francisco, San Francisco General Hospital
mi
from
San Francisco, CA
Click here to add this to my saved trials
Pragmatic, Randomized Evaluation of Statin Active Choice to Reach Improved Outcomes Based on Evidence
Pragmatic, Randomized Evaluation of Statin Active Choice to Reach Improved Outcomes Based on Evidence
Status: Enrolling
Updated:  5/1/2017
University of Pennsylvania Health System
mi
from
Philadelphia, PA
Pragmatic, Randomized Evaluation of Statin Active Choice to Reach Improved Outcomes Based on Evidence
Pragmatic, Randomized Evaluation of Statin Active Choice to Reach Improved Outcomes Based on Evidence
Status: Enrolling
Updated: 5/1/2017
University of Pennsylvania Health System
mi
from
Philadelphia, PA
Click here to add this to my saved trials
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
Status: Enrolling
Updated:  5/2/2017
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
Status: Enrolling
Updated: 5/2/2017
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
Click here to add this to my saved trials
Antiplatelet Activity of Aspirin in Infants After Aortopulmonary and Cavopulmonary Shunts
Antiplatelet Activity of Aspirin in Infants After Aortopulmonary and Cavopulmonary Shunts
Status: Enrolling
Updated:  5/4/2017
Primary Children's Medical Center
mi
from
Salt Lake City, UT
Antiplatelet Activity of Aspirin in Infants After Aortopulmonary and Cavopulmonary Shunts
Antiplatelet Activity of Aspirin in Infants After Aortopulmonary and Cavopulmonary Shunts
Status: Enrolling
Updated: 5/4/2017
Primary Children's Medical Center
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Canadian Cardiology de Novo Study: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens
Clinical and Laboratory Evaluation of Acute Rejection, Myocyte Growth, Repair, and Oxidative Stress Following de Novo Cardiac Transplant: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens With MPA TDM
Status: Enrolling
Updated:  5/4/2017
Clinical Research Facility
mi
from
Los Angeles, CA
Canadian Cardiology de Novo Study: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens
Clinical and Laboratory Evaluation of Acute Rejection, Myocyte Growth, Repair, and Oxidative Stress Following de Novo Cardiac Transplant: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens With MPA TDM
Status: Enrolling
Updated: 5/4/2017
Clinical Research Facility
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Canadian Cardiology de Novo Study: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens
Clinical and Laboratory Evaluation of Acute Rejection, Myocyte Growth, Repair, and Oxidative Stress Following de Novo Cardiac Transplant: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens With MPA TDM
Status: Enrolling
Updated:  5/4/2017
mi
from
Calgary,
Canadian Cardiology de Novo Study: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens
Clinical and Laboratory Evaluation of Acute Rejection, Myocyte Growth, Repair, and Oxidative Stress Following de Novo Cardiac Transplant: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens With MPA TDM
Status: Enrolling
Updated: 5/4/2017
mi
from
Calgary,
Click here to add this to my saved trials
IMPACT: Inactivity Monitoring and Physical Activity Controlled Trial
IMPACT: Inactivity Monitoring and Physical Activity Controlled Trial
Status: Enrolling
Updated:  5/10/2017
University of Texas Medical Branch
mi
from
Galveston, TX
IMPACT: Inactivity Monitoring and Physical Activity Controlled Trial
IMPACT: Inactivity Monitoring and Physical Activity Controlled Trial
Status: Enrolling
Updated: 5/10/2017
University of Texas Medical Branch
mi
from
Galveston, TX
Click here to add this to my saved trials
A Comparison of Hemorrhagic and Ischemic Strokes Among Blacks and Whites
A Comparison of Hemorrhagic and Ischemic Strokes Among Blacks and Whites: A Population-Based Study in Cincinnati, Ohio
Status: Enrolling
Updated:  5/11/2017
University of Cincinnati
mi
from
Cincinnati, OH
A Comparison of Hemorrhagic and Ischemic Strokes Among Blacks and Whites
A Comparison of Hemorrhagic and Ischemic Strokes Among Blacks and Whites: A Population-Based Study in Cincinnati, Ohio
Status: Enrolling
Updated: 5/11/2017
University of Cincinnati
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Patients' Perspectives of Factors That Support the Management of Peripheral Arterial Disease for Improved Outcomes
A Study of Patients' Perspectives of Factors That Support the Management of Cardiac Care for Improved Outcomes in a Peripheral Arterial Disease Population
Status: Enrolling
Updated:  5/22/2017
VA ECHCS
mi
from
Denver, CO
Patients' Perspectives of Factors That Support the Management of Peripheral Arterial Disease for Improved Outcomes
A Study of Patients' Perspectives of Factors That Support the Management of Cardiac Care for Improved Outcomes in a Peripheral Arterial Disease Population
Status: Enrolling
Updated: 5/22/2017
VA ECHCS
mi
from
Denver, CO
Click here to add this to my saved trials
Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy
A Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy for the Treatment of Coronary Artery Disease Using Direct Intramyocardial Administration of an Adenovirus Vector Expressing the VEGF121 cDNA
Status: Enrolling
Updated:  5/23/2017
Stony Brook University Medical Center
mi
from
Stony Brook, NY
Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy
A Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy for the Treatment of Coronary Artery Disease Using Direct Intramyocardial Administration of an Adenovirus Vector Expressing the VEGF121 cDNA
Status: Enrolling
Updated: 5/23/2017
Stony Brook University Medical Center
mi
from
Stony Brook, NY
Click here to add this to my saved trials
Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy
A Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy for the Treatment of Coronary Artery Disease Using Direct Intramyocardial Administration of an Adenovirus Vector Expressing the VEGF121 cDNA
Status: Enrolling
Updated:  5/23/2017
Weill Cornell Medicine
mi
from
New York, NY
Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy
A Post Ten Year Follow up Assessment of a Phase I Trial of Angiogenic Gene Therapy for the Treatment of Coronary Artery Disease Using Direct Intramyocardial Administration of an Adenovirus Vector Expressing the VEGF121 cDNA
Status: Enrolling
Updated: 5/23/2017
Weill Cornell Medicine
mi
from
New York, NY
Click here to add this to my saved trials
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated:  6/1/2017
Aurora Bay Care
mi
from
Green Bay, WI
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated: 6/1/2017
Aurora Bay Care
mi
from
Green Bay, WI
Click here to add this to my saved trials
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated:  6/1/2017
University of Wisconsin-Madison
mi
from
Madison, WI
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated: 6/1/2017
University of Wisconsin-Madison
mi
from
Madison, WI
Click here to add this to my saved trials
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated:  6/1/2017
Marshfield Clinic
mi
from
Marshfield, WI
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated: 6/1/2017
Marshfield Clinic
mi
from
Marshfield, WI
Click here to add this to my saved trials
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated:  6/1/2017
Gundersen Lutheran
mi
from
La Crosse, WI
Study of Cardiovascular Disease and Obstructive Sleep Apnea
Pharmacologic Interventions for Cardiovascular Disease in Obstructive Sleep Apnea
Status: Enrolling
Updated: 6/1/2017
Gundersen Lutheran
mi
from
La Crosse, WI
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Arizona Center for Neurosurgery
mi
from
Phoenix, AZ
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Arizona Center for Neurosurgery
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Tucson Orthopaedic Institute
mi
from
Tucson, AZ
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Tucson Orthopaedic Institute
mi
from
Tucson, AZ
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
D.I.S.C. Sports and Spine Center
mi
from
Beverly Hills, CA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
D.I.S.C. Sports and Spine Center
mi
from
Beverly Hills, CA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Tower Orthopaedics and Sports Medicine/ Institute for Advanced Spinal Research
mi
from
Beverly Hills, CA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Tower Orthopaedics and Sports Medicine/ Institute for Advanced Spinal Research
mi
from
Beverly Hills, CA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Brain and Spine Research Institute
mi
from
Los Angeles, CA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Brain and Spine Research Institute
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Pacific Pain Medicine Consultants/Pacific Surgery Center
mi
from
Oceanside, CA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Pacific Pain Medicine Consultants/Pacific Surgery Center
mi
from
Oceanside, CA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Orange County Neurosurgical Associates
mi
from
Orange County, CA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Orange County Neurosurgical Associates
mi
from
Orange County, CA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
University of Colorado Hospital- The Spine Center- Anshutz Outpatient Pavilion
mi
from
Aurora, CO
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
University of Colorado Hospital- The Spine Center- Anshutz Outpatient Pavilion
mi
from
Aurora, CO
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Durango Orthopedic Associates, P.C./Spine Colorado
mi
from
Durango, CO
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Durango Orthopedic Associates, P.C./Spine Colorado
mi
from
Durango, CO
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Colorado Spine And Scoliosis Institute
mi
from
Littleton, CO
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Colorado Spine And Scoliosis Institute
mi
from
Littleton, CO
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Yale University
mi
from
New Haven, CT
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Yale University
mi
from
New Haven, CT
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Florida Research Associates, LLC
mi
from
Deland, FL
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Florida Research Associates, LLC
mi
from
Deland, FL
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Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Shrock Orthopedic Research, LLC
mi
from
Fort Lauderdale, FL
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Shrock Orthopedic Research, LLC
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Rush University Medical Center
mi
from
Chicago, IL
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Rush University Medical Center
mi
from
Chicago, IL
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Spine Institute of Louisiana
mi
from
Shreveport, LA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Spine Institute of Louisiana
mi
from
Shreveport, LA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Greater Baltimore Neurosurgical Associates at GBMA
mi
from
Baltimore, MD
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Greater Baltimore Neurosurgical Associates at GBMA
mi
from
Baltimore, MD
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Sports Medicine North
mi
from
Peabody, MA
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Sports Medicine North
mi
from
Peabody, MA
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Institute for Low Back and Neck Care
mi
from
Minneapolis, MN
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Institute for Low Back and Neck Care
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Orthopedics Associates of the Greater Lehigh Valley
mi
from
Phillipsburg, NJ
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Orthopedics Associates of the Greater Lehigh Valley
mi
from
Phillipsburg, NJ
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Spine Care and Rehabilitation, Inc.
mi
from
Roseland, NJ
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Spine Care and Rehabilitation, Inc.
mi
from
Roseland, NJ
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Stony Brook University Medical Center, Dept. of Neurological Surgery
mi
from
Stony Brook, NY
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Stony Brook University Medical Center, Dept. of Neurological Surgery
mi
from
Stony Brook, NY
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Upstate Medical Universtiy-Department of Orthopedics- Institute for Spine Care
mi
from
Syracuse, NY
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Upstate Medical Universtiy-Department of Orthopedics- Institute for Spine Care
mi
from
Syracuse, NY
Click here to add this to my saved trials
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated:  6/6/2017
Triangle Orthopaedic Associates
mi
from
Durham, NC
Investigating Superion™ In Spinal Stenosis
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis
Status: Enrolling
Updated: 6/6/2017
Triangle Orthopaedic Associates
mi
from
Durham, NC
Click here to add this to my saved trials