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

Dynamic Substrate Mapping (DSM) for Ischemic VT
Clinical Feasibility of Using Dynamic Substrate Mapping to Guide Ablation of Ischemic Ventricular Tachycardia
Status: Enrolling
Updated:  12/31/1969
Northwestern University
mi
from
Chicago, IL
Dynamic Substrate Mapping (DSM) for Ischemic VT
Clinical Feasibility of Using Dynamic Substrate Mapping to Guide Ablation of Ischemic Ventricular Tachycardia
Status: Enrolling
Updated: 12/31/1969
Northwestern University
mi
from
Chicago, IL
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Dynamic Substrate Mapping (DSM) for Ischemic VT
Clinical Feasibility of Using Dynamic Substrate Mapping to Guide Ablation of Ischemic Ventricular Tachycardia
Status: Enrolling
Updated:  12/31/1969
Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
Dynamic Substrate Mapping (DSM) for Ischemic VT
Clinical Feasibility of Using Dynamic Substrate Mapping to Guide Ablation of Ischemic Ventricular Tachycardia
Status: Enrolling
Updated: 12/31/1969
Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
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Dynamic Substrate Mapping (DSM) for Ischemic VT
Clinical Feasibility of Using Dynamic Substrate Mapping to Guide Ablation of Ischemic Ventricular Tachycardia
Status: Enrolling
Updated:  12/31/1969
Sentara Norfolk General Hospital
mi
from
Norfolk, VA
Dynamic Substrate Mapping (DSM) for Ischemic VT
Clinical Feasibility of Using Dynamic Substrate Mapping to Guide Ablation of Ischemic Ventricular Tachycardia
Status: Enrolling
Updated: 12/31/1969
Sentara Norfolk General Hospital
mi
from
Norfolk, VA
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Good Samaritan Hospital
mi
from
Los Angeles, CA
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Good Samaritan Hospital
mi
from
Los Angeles, CA
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Michigan Heart, PC
mi
from
Ypsilanti, MI
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Michigan Heart, PC
mi
from
Ypsilanti, MI
Click here to add this to my saved trials
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
The Cooper Health System
mi
from
Camden, NJ
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
The Cooper Health System
mi
from
Camden, NJ
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Wake Forest University Baptist Medical Center
mi
from
Winston-Salem, NC
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Wake Forest University Baptist Medical Center
mi
from
Winston-Salem, NC
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Altru Health System Hospital
mi
from
Grand Forks, ND
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Altru Health System Hospital
mi
from
Grand Forks, ND
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Ohiohealth Research Institute @ Riverside Methodist Hospital
mi
from
Columbus, OH
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Ohiohealth Research Institute @ Riverside Methodist Hospital
mi
from
Columbus, OH
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Providence Health & Services
mi
from
Portland, OR
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Providence Health & Services
mi
from
Portland, OR
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Main Line Health Heart Center: Bryn Mawr Hospital
mi
from
Bryn Mawr, PA
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Main Line Health Heart Center: Bryn Mawr Hospital
mi
from
Bryn Mawr, PA
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Main Line Health Heart Center: Lankenau Hospitals
mi
from
Wynnewood, PA
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Main Line Health Heart Center: Lankenau Hospitals
mi
from
Wynnewood, PA
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Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated:  12/31/1969
Baptist Hospital West
mi
from
Knoxville, TN
Angio-Seal Evolution Device Registry
Clinical Registry of the St. Jude Medical Angio-Seal(TM) Evolution(TM) Vascular Closure Device Following Diagnostic and/or Interventional Endovascular Procedures
Status: Enrolling
Updated: 12/31/1969
Baptist Hospital West
mi
from
Knoxville, TN
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Anchorage, AK
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Anchorage, AK
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Brandon, FL
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Brandon, FL
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Orlando, FL
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Orlando, FL
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Davenport, IA
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Davenport, IA
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Boston, MA
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Boston, MA
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Minneapolis, MN
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Minneapolis, MN
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Kansas City, MO
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Kansas City, MO
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Mineola, NY
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Mineola, NY
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Stony Brook, NY
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Stony Brook, NY
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Gastonia, NC
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Gastonia, NC
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Raleigh, NC
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Raleigh, NC
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Nashville, TN
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Nashville, TN
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ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Austin, TX
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Austin, TX
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Burlington, VT
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Burlington, VT
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Richmond, VA
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Richmond, VA
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Morgantown, WV
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Morgantown, WV
Click here to add this to my saved trials
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated:  12/31/1969
mi
from
Linz,
ST Segment Detection Study
ST Segment Detection Study
Status: Enrolling
Updated: 12/31/1969
mi
from
Linz,
Click here to add this to my saved trials
Plant-Based, American Heart Assoc. or Mediterranean Diets In 9-18 yo With BMI >95%, Cholesterol >169 and Their Parents
Plant-Based, No-Added-Fat or American Heart Association or Mediterranean Diets a Prospective Randomized Trial: Impact on Cardiovascular Risk in Obese Children With Hypercholesterolemia and in One of Their Parents
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
Plant-Based, American Heart Assoc. or Mediterranean Diets In 9-18 yo With BMI >95%, Cholesterol >169 and Their Parents
Plant-Based, No-Added-Fat or American Heart Association or Mediterranean Diets a Prospective Randomized Trial: Impact on Cardiovascular Risk in Obese Children With Hypercholesterolemia and in One of Their Parents
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
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Detection of Cerebral Ischemia With a Noninvasive Neurometabolic Optical Monitor
Detection of Cerebral Ischemia With a Noninvasive Neurometabolic Optical Monitor
Status: Enrolling
Updated:  12/31/1969
University of Pennylvania Health System
mi
from
Philadelphia, PA
Detection of Cerebral Ischemia With a Noninvasive Neurometabolic Optical Monitor
Detection of Cerebral Ischemia With a Noninvasive Neurometabolic Optical Monitor
Status: Enrolling
Updated: 12/31/1969
University of Pennylvania Health System
mi
from
Philadelphia, PA
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The Effects of Interrupting Prolonged Sitting With Intermittent Exercise on Postprandial Lipemia
The Effects of Interrupting Prolonged Sitting With Intermittent Exercise on Postprandial Lipemia
Status: Enrolling
Updated:  12/31/1969
University of Texas at Austin Human Performance Laboratory
mi
from
Austin, TX
The Effects of Interrupting Prolonged Sitting With Intermittent Exercise on Postprandial Lipemia
The Effects of Interrupting Prolonged Sitting With Intermittent Exercise on Postprandial Lipemia
Status: Enrolling
Updated: 12/31/1969
University of Texas at Austin Human Performance Laboratory
mi
from
Austin, TX
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ConnectedHeartHealth - Heart Failure Readmission Intervention
ConnectedHeartHealth - Heart Failure Readmission Intervention
Status: Enrolling
Updated:  12/31/1969
Sinai Hospital of Baltimore
mi
from
Baltimore, MD
ConnectedHeartHealth - Heart Failure Readmission Intervention
ConnectedHeartHealth - Heart Failure Readmission Intervention
Status: Enrolling
Updated: 12/31/1969
Sinai Hospital of Baltimore
mi
from
Baltimore, MD
Click here to add this to my saved trials
Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)
A Multicenter Open-Label Extension (OLE) Study To Assess The Long-Term Safety and Efficacy of Bempedoic Acid (ETC-1002) 180 MG
Status: Enrolling
Updated:  12/31/1969
Jedidiah Clinical Research
mi
from
Tampa, FL
Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)
A Multicenter Open-Label Extension (OLE) Study To Assess The Long-Term Safety and Efficacy of Bempedoic Acid (ETC-1002) 180 MG
Status: Enrolling
Updated: 12/31/1969
Jedidiah Clinical Research
mi
from
Tampa, FL
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Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)
A Multicenter Open-Label Extension (OLE) Study To Assess The Long-Term Safety and Efficacy of Bempedoic Acid (ETC-1002) 180 MG
Status: Enrolling
Updated:  12/31/1969
L-MARC Research Center
mi
from
Louisville, KY
Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)
A Multicenter Open-Label Extension (OLE) Study To Assess The Long-Term Safety and Efficacy of Bempedoic Acid (ETC-1002) 180 MG
Status: Enrolling
Updated: 12/31/1969
L-MARC Research Center
mi
from
Louisville, KY
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Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)
A Multicenter Open-Label Extension (OLE) Study To Assess The Long-Term Safety and Efficacy of Bempedoic Acid (ETC-1002) 180 MG
Status: Enrolling
Updated:  12/31/1969
Sentral Clinical Research Services, LLC
mi
from
Cincinnati, OH
Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)
A Multicenter Open-Label Extension (OLE) Study To Assess The Long-Term Safety and Efficacy of Bempedoic Acid (ETC-1002) 180 MG
Status: Enrolling
Updated: 12/31/1969
Sentral Clinical Research Services, LLC
mi
from
Cincinnati, OH
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Bioequivalence Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers
An Open-Label, Randomized, Two-Treatment, Two-Sequence, Four-Period, Fully Replicated Crossover Bioequivalence Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Bio-Kinetic Clinical Applications, Inc.
mi
from
Springfield, MO
Bioequivalence Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers
An Open-Label, Randomized, Two-Treatment, Two-Sequence, Four-Period, Fully Replicated Crossover Bioequivalence Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Bio-Kinetic Clinical Applications, Inc.
mi
from
Springfield, MO
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Healthy Hearts Healthy Minds
Healthy Hearts Healthy Minds: A PPRN Demonstration Pragmatic Trial
Status: Enrolling
Updated:  12/31/1969
Dauten Family Center for Bipolar Treatment Innovation
mi
from
Boston, MA
Healthy Hearts Healthy Minds
Healthy Hearts Healthy Minds: A PPRN Demonstration Pragmatic Trial
Status: Enrolling
Updated: 12/31/1969
Dauten Family Center for Bipolar Treatment Innovation
mi
from
Boston, MA
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Real Time Myocardial Contrast Echocardiography and Dobutamine Stress Perfusion Magnetic Resonance Imaging
Quantification of Ventricular Mechanics/Myocardial Blood Flow Reserve in Adolescents and Adults Ages 12-50 With Congenital or Acquired Heart Disease Using Bicycle Stress With Real Time Myocardial Contrast Echo and Dobutamine Stress MRI
Status: Enrolling
Updated:  12/31/1969
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
Real Time Myocardial Contrast Echocardiography and Dobutamine Stress Perfusion Magnetic Resonance Imaging
Quantification of Ventricular Mechanics/Myocardial Blood Flow Reserve in Adolescents and Adults Ages 12-50 With Congenital or Acquired Heart Disease Using Bicycle Stress With Real Time Myocardial Contrast Echo and Dobutamine Stress MRI
Status: Enrolling
Updated: 12/31/1969
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
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The Effect of Anesthesia on Neurodevelopmental Outcome (NDO)
Anesthesia and the Developing Brain: a Comparison of Two Anesthetic Techniques
Status: Enrolling
Updated:  12/31/1969
Stanford Children's Hospital
mi
from
Palo Alto, CA
The Effect of Anesthesia on Neurodevelopmental Outcome (NDO)
Anesthesia and the Developing Brain: a Comparison of Two Anesthetic Techniques
Status: Enrolling
Updated: 12/31/1969
Stanford Children's Hospital
mi
from
Palo Alto, CA
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Validation of a Diet Risk Screening Tool
Validation of a Diet Risk Screening Tool
Status: Enrolling
Updated:  12/31/1969
Pennsylvania State University
mi
from
University Park, PA
Validation of a Diet Risk Screening Tool
Validation of a Diet Risk Screening Tool
Status: Enrolling
Updated: 12/31/1969
Pennsylvania State University
mi
from
University Park, PA
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BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
Vascular Breakthroughs
mi
from
Darien, CT
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
Vascular Breakthroughs
mi
from
Darien, CT
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BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
Yale University
mi
from
New Haven, CT
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
Yale University
mi
from
New Haven, CT
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BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
Midwest Cardiovascular Research Foundation
mi
from
Davenport, IA
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
Midwest Cardiovascular Research Foundation
mi
from
Davenport, IA
Click here to add this to my saved trials
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
Metro Health Hospital
mi
from
Wyoming, MI
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
Metro Health Hospital
mi
from
Wyoming, MI
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BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
Cox Medical Centers
mi
from
Springfield, MO
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
Cox Medical Centers
mi
from
Springfield, MO
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BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
Mount Sinai Hospital
mi
from
New York, NY
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
Mount Sinai Hospital
mi
from
New York, NY
Click here to add this to my saved trials
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated:  12/31/1969
North Carolina Heart and Vascular
mi
from
Raleigh, NC
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
The BARD® VENOVO™ Venous Stent Study - A Prospective, Non-Randomized, Multi-Center, Single-Arm Study of the Treatment of Iliofemoral Occlusive Disease - an Assessment for Effectiveness and Safety (VERNACULAR)
Status: Enrolling
Updated: 12/31/1969
North Carolina Heart and Vascular
mi
from
Raleigh, NC
Click here to add this to my saved trials