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
31,654
archived clinical trials in
Cardiology

Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
Wheaton Franciscan All Saints
mi
from
Racine, WI
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
Wheaton Franciscan All Saints
mi
from
Racine, WI
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Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
Florida Hospital
mi
from
Orlando, FL
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
Florida Hospital
mi
from
Orlando, FL
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Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
University of Massachusetts-Worchester
mi
from
Worcester, MA
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
University of Massachusetts-Worchester
mi
from
Worcester, MA
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Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
Michigan Heart, PC
mi
from
Ypsilanti, MI
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
Michigan Heart, PC
mi
from
Ypsilanti, MI
Click here to add this to my saved trials
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
Doylestown Health Cardiology/Central Bucks
mi
from
Doylestown, PA
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
Doylestown Health Cardiology/Central Bucks
mi
from
Doylestown, PA
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Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
Marshfield Clinic
mi
from
Marshfield, WI
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
Marshfield Clinic
mi
from
Marshfield, WI
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Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
University of Calgary
mi
from
Calgary,
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
University of Calgary
mi
from
Calgary,
Click here to add this to my saved trials
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
Sequoia Hospital
mi
from
East Palo Alto, CA
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
Sequoia Hospital
mi
from
East Palo Alto, CA
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Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated:  12/31/1969
University of Florida/Cardiovascular Medicine
mi
from
Gainesville, FL
Ranolazine Implantable Cardioverter-Defibrillator Trial
Late Sodium Current Blockade in High-Risk ICD Patients
Status: Enrolling
Updated: 12/31/1969
University of Florida/Cardiovascular Medicine
mi
from
Gainesville, FL
Click here to add this to my saved trials
Clinical Pharmacology of Aliskiren in Combination With Cyclosporine in Cardiac Transplantation
Clinical Pharmacology of Aliskiren in Combination With Cyclosporine in Cardiac Transplantation
Status: Enrolling
Updated:  12/31/1969
University of Colorado Denver
mi
from
Aurora, CO
Clinical Pharmacology of Aliskiren in Combination With Cyclosporine in Cardiac Transplantation
Clinical Pharmacology of Aliskiren in Combination With Cyclosporine in Cardiac Transplantation
Status: Enrolling
Updated: 12/31/1969
University of Colorado Denver
mi
from
Aurora, CO
Click here to add this to my saved trials
Randomized Evaluation of Patients With Stable Angina Comparing Diagnostic Examinations
ACRIN 4701 RESCUE: Randomized Evaluation of Patients With Stable Angina Comparing Utilization of Diagnostic Examinations
Status: Enrolling
Updated:  12/31/1969
Atlantic VA Medical Center
mi
from
Decatur, GA
Randomized Evaluation of Patients With Stable Angina Comparing Diagnostic Examinations
ACRIN 4701 RESCUE: Randomized Evaluation of Patients With Stable Angina Comparing Utilization of Diagnostic Examinations
Status: Enrolling
Updated: 12/31/1969
Atlantic VA Medical Center
mi
from
Decatur, GA
Click here to add this to my saved trials
Randomized Evaluation of Patients With Stable Angina Comparing Diagnostic Examinations
ACRIN 4701 RESCUE: Randomized Evaluation of Patients With Stable Angina Comparing Utilization of Diagnostic Examinations
Status: Enrolling
Updated:  12/31/1969
Henry Ford Hospital
mi
from
Detroit, MI
Randomized Evaluation of Patients With Stable Angina Comparing Diagnostic Examinations
ACRIN 4701 RESCUE: Randomized Evaluation of Patients With Stable Angina Comparing Utilization of Diagnostic Examinations
Status: Enrolling
Updated: 12/31/1969
Henry Ford Hospital
mi
from
Detroit, MI
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Randomized Evaluation of Patients With Stable Angina Comparing Diagnostic Examinations
ACRIN 4701 RESCUE: Randomized Evaluation of Patients With Stable Angina Comparing Utilization of Diagnostic Examinations
Status: Enrolling
Updated:  12/31/1969
Salem VA Medical Center
mi
from
Salem, VA
Randomized Evaluation of Patients With Stable Angina Comparing Diagnostic Examinations
ACRIN 4701 RESCUE: Randomized Evaluation of Patients With Stable Angina Comparing Utilization of Diagnostic Examinations
Status: Enrolling
Updated: 12/31/1969
Salem VA Medical Center
mi
from
Salem, VA
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Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
Florida Hospital
mi
from
Orlando, FL
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
Florida Hospital
mi
from
Orlando, FL
Click here to add this to my saved trials
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
Northwestern Hospital
mi
from
Chicago, IL
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
Northwestern Hospital
mi
from
Chicago, IL
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Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
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Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
Cooper University Hospital
mi
from
Camden, NJ
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
Cooper University Hospital
mi
from
Camden, NJ
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Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
Saint Thomas Health
mi
from
Nashville, TN
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
Saint Thomas Health
mi
from
Nashville, TN
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Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
The John Paul II Hospital in Krakow
mi
from
Krakow,
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
The John Paul II Hospital in Krakow
mi
from
Krakow,
Click here to add this to my saved trials
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated:  12/31/1969
Washington University
mi
from
Saint Louis, MO
Magna Mitral - 23mm
Clinical Evaluation of the Size 23mm Carpentier-Edwards PERIMOUNT Magna Mitral Bioprosthesis, Model 7000TFX
Status: Enrolling
Updated: 12/31/1969
Washington University
mi
from
Saint Louis, MO
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Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Fremont, CA
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Fremont, CA
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
New Haven, CT
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
New Haven, CT
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Rockford, IL
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Rockford, IL
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Munster, IN
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Munster, IN
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Houma, LA
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Houma, LA
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Lansing, MI
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Lansing, MI
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Saginaw, MI
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Saginaw, MI
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Wyoming, MI
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Wyoming, MI
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Ypsilanti, MI
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Ypsilanti, MI
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Tupelo, MS
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Tupelo, MS
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Kansas City, MO
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Kansas City, MO
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Ridgewood, NJ
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Ridgewood, NJ
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
New York, NY
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
New York, NY
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Gastonia, NC
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Gastonia, NC
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
High Point, NC
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
High Point, NC
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Toledo, OH
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Toledo, OH
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Toledo, OH
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Toledo, OH
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Doylestown, PA
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Doylestown, PA
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Langhorne, PA
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Langhorne, PA
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Pittsburgh, PA
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Pittsburgh, PA
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Providence, RI
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Providence, RI
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Greenville, SC
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Greenville, SC
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Rock Hill, SC
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Rock Hill, SC
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Kingsport, TN
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Kingsport, TN
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Amarillo, TX
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Amarillo, TX
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Austin, TX
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Austin, TX
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
McKinney, TX
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
McKinney, TX
Click here to add this to my saved trials
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Tyler, TX
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
The Treatment of Iliac and Femoral Atherosclerotic Lesions Using the Self-expanding Astron and Pulsar Stents
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Tyler, TX
Click here to add this to my saved trials