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

An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Saint Luke's Mid America Heart and Vascular Institute
mi
from
Kansas City, MO
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Saint Luke's Mid America Heart and Vascular Institute
mi
from
Kansas City, MO
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An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Columbia University Medical Center
mi
from
New York City, NY
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Columbia University Medical Center
mi
from
New York City, NY
Click here to add this to my saved trials
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Lenox Hill Hospital
mi
from
New York, NY
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Lenox Hill Hospital
mi
from
New York, NY
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An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
University of Toledo
mi
from
Toledo, OH
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
University of Toledo
mi
from
Toledo, OH
Click here to add this to my saved trials
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Temple University Hospital
mi
from
Philadelphia, PA
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Temple University Hospital
mi
from
Philadelphia, PA
Click here to add this to my saved trials
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Scott & White Memorial Hospital
mi
from
Temple, TX
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Scott & White Memorial Hospital
mi
from
Temple, TX
Click here to add this to my saved trials
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Mayo Clinic, Jacksonville
mi
from
Jacksonville, FL
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Mayo Clinic, Jacksonville
mi
from
Jacksonville, FL
Click here to add this to my saved trials
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Florida Hospital
mi
from
Orlando, FL
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Florida Hospital
mi
from
Orlando, FL
Click here to add this to my saved trials
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated:  7/27/2015
Emory University
mi
from
Atlanta, GA
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery
An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial
Status: Enrolling
Updated: 7/27/2015
Emory University
mi
from
Atlanta, GA
Click here to add this to my saved trials
Coronary Heart Disease as Measured by Coronary Calcium Score Among Individuals With Chronic Traumatic Spinal Cord Injury
Prevalence and Risk of Coronary Heart Disease as Measured by Coronary Calcium Score Among Individuals With Chronic Traumatic Spinal Cord Injury(SCI): A Pilot Study
Status: Enrolling
Updated:  7/27/2015
Carolinas Rehabilitation
mi
from
Charlotte, NC
Coronary Heart Disease as Measured by Coronary Calcium Score Among Individuals With Chronic Traumatic Spinal Cord Injury
Prevalence and Risk of Coronary Heart Disease as Measured by Coronary Calcium Score Among Individuals With Chronic Traumatic Spinal Cord Injury(SCI): A Pilot Study
Status: Enrolling
Updated: 7/27/2015
Carolinas Rehabilitation
mi
from
Charlotte, NC
Click here to add this to my saved trials
Pharmacokinetics of Tranexamic Acid (TXA) in Children Undergoing Repair of Congenital Heart Defects Utilizing Cardiopulmonary Bypass
Pharmacokinetics of Tranexamic Acid (TXA) in Children Undergoing Repair of Congenital Heart Defects Utilizing Cardiopulmonary Bypass
Status: Enrolling
Updated:  7/29/2015
Children's Hospital Boston
mi
from
Boston, MA
Pharmacokinetics of Tranexamic Acid (TXA) in Children Undergoing Repair of Congenital Heart Defects Utilizing Cardiopulmonary Bypass
Pharmacokinetics of Tranexamic Acid (TXA) in Children Undergoing Repair of Congenital Heart Defects Utilizing Cardiopulmonary Bypass
Status: Enrolling
Updated: 7/29/2015
Children's Hospital Boston
mi
from
Boston, MA
Click here to add this to my saved trials
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Status: Enrolling
Updated:  7/30/2015
Yale University
mi
from
New Haven, CT
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Status: Enrolling
Updated: 7/30/2015
Yale University
mi
from
New Haven, CT
Click here to add this to my saved trials
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Status: Enrolling
Updated:  7/30/2015
University of Indiana
mi
from
Indianapolis, IN
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Sleep Apnea in TIA/Stroke: Reducing Cardiovascular Risk With Positive Airway Pressure
Status: Enrolling
Updated: 7/30/2015
University of Indiana
mi
from
Indianapolis, IN
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Length of Effect of Extended Release Aspirin on Platelets in Patients With Diabetes and Heart Disease
Durability of Antiplatelet Effect of a Novel Extended-Release Formulation of Acetylsalicylic Acid, Durlaza in CVD (Cardiovascular Disease) Patients at Risk of High Platelet Turnover
Status: Enrolling
Updated:  8/4/2015
Platelet and Thrombosis Research, LLC
mi
from
Baltimore, MD
Length of Effect of Extended Release Aspirin on Platelets in Patients With Diabetes and Heart Disease
Durability of Antiplatelet Effect of a Novel Extended-Release Formulation of Acetylsalicylic Acid, Durlaza in CVD (Cardiovascular Disease) Patients at Risk of High Platelet Turnover
Status: Enrolling
Updated: 8/4/2015
Platelet and Thrombosis Research, LLC
mi
from
Baltimore, MD
Click here to add this to my saved trials
Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy
Virtual Left Ventricular Lead Navigation in Patients With Ischemic Cardiomyopathy
Status: Enrolling
Updated:  8/5/2015
UPMC Presbyterian Hospital
mi
from
Pittsburgh, PA
Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy
Virtual Left Ventricular Lead Navigation in Patients With Ischemic Cardiomyopathy
Status: Enrolling
Updated: 8/5/2015
UPMC Presbyterian Hospital
mi
from
Pittsburgh, PA
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Interactive Cholesterol Advisory Tool
The Interactive Cholesterol Advisory Tool
Status: Enrolling
Updated:  8/5/2015
University of Rochester
mi
from
Rochester, NY
Interactive Cholesterol Advisory Tool
The Interactive Cholesterol Advisory Tool
Status: Enrolling
Updated: 8/5/2015
University of Rochester
mi
from
Rochester, NY
Click here to add this to my saved trials
Pilot Study of PRT-201 Following Angioplasty in Patients With Peripheral Artery Disease (PAD)
Open-Label, Dose-Escalation, Pilot Study of PRT-201 Administered Following Angioplasty in Patients With Peripheral Artery Disease in the Lower Extremity
Status: Enrolling
Updated:  8/7/2015
San Francisco VA Medical Center
mi
from
San Francisco, CA
Pilot Study of PRT-201 Following Angioplasty in Patients With Peripheral Artery Disease (PAD)
Open-Label, Dose-Escalation, Pilot Study of PRT-201 Administered Following Angioplasty in Patients With Peripheral Artery Disease in the Lower Extremity
Status: Enrolling
Updated: 8/7/2015
San Francisco VA Medical Center
mi
from
San Francisco, CA
Click here to add this to my saved trials
Pilot Study of PRT-201 Following Angioplasty in Patients With Peripheral Artery Disease (PAD)
Open-Label, Dose-Escalation, Pilot Study of PRT-201 Administered Following Angioplasty in Patients With Peripheral Artery Disease in the Lower Extremity
Status: Enrolling
Updated:  8/7/2015
University of California, San Francisco Medical Center
mi
from
San Francisco, CA
Pilot Study of PRT-201 Following Angioplasty in Patients With Peripheral Artery Disease (PAD)
Open-Label, Dose-Escalation, Pilot Study of PRT-201 Administered Following Angioplasty in Patients With Peripheral Artery Disease in the Lower Extremity
Status: Enrolling
Updated: 8/7/2015
University of California, San Francisco Medical Center
mi
from
San Francisco, CA
Click here to add this to my saved trials
WalkLink: Internet-based Walking Program
WalkLink:Internet-based Walking Program for Cardiovascular Disease Risk-Reduction
Status: Enrolling
Updated:  8/12/2015
Penn State College of Medicine, Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
WalkLink: Internet-based Walking Program
WalkLink:Internet-based Walking Program for Cardiovascular Disease Risk-Reduction
Status: Enrolling
Updated: 8/12/2015
Penn State College of Medicine, Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
Click here to add this to my saved trials
A Lifestyle Physical Activity Intervention for Older Sedentary Women
A Lifestyle Physical Activity Intervention for Older Sedentary Women
Status: Enrolling
Updated:  8/13/2015
University of Arkansas for Medical Sciences
mi
from
Little Rock, AR
A Lifestyle Physical Activity Intervention for Older Sedentary Women
A Lifestyle Physical Activity Intervention for Older Sedentary Women
Status: Enrolling
Updated: 8/13/2015
University of Arkansas for Medical Sciences
mi
from
Little Rock, AR
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Determination of Fractional Flow Reserve by Anatomic Computed Tomographic Angiography
Determination of Fractional Flow Reserve by Anatomic Computed Tomographic Angiography
Status: Enrolling
Updated:  8/17/2015
Spring Hill Hospital
mi
from
Mobile, AL
Determination of Fractional Flow Reserve by Anatomic Computed Tomographic Angiography
Determination of Fractional Flow Reserve by Anatomic Computed Tomographic Angiography
Status: Enrolling
Updated: 8/17/2015
Spring Hill Hospital
mi
from
Mobile, AL
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Veterans Walk for Health Study
Does Step Count Feedback Enhance Counseling for Weight Loss?
Status: Enrolling
Updated:  8/19/2015
VA Ann Arbor Healthcare System, Ann Arbor, MI
mi
from
Ann Arbor, MI
Veterans Walk for Health Study
Does Step Count Feedback Enhance Counseling for Weight Loss?
Status: Enrolling
Updated: 8/19/2015
VA Ann Arbor Healthcare System, Ann Arbor, MI
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Parenting After Infant Congenital Heart Defect Diagnosis
Parenting After Infant Congenital Heart Defect Diagnosis
Status: Enrolling
Updated:  8/19/2015
University of Wisconsin-Madison
mi
from
Madison, WI
Parenting After Infant Congenital Heart Defect Diagnosis
Parenting After Infant Congenital Heart Defect Diagnosis
Status: Enrolling
Updated: 8/19/2015
University of Wisconsin-Madison
mi
from
Madison, WI
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Parenting After Infant Congenital Heart Defect Diagnosis
Parenting After Infant Congenital Heart Defect Diagnosis
Status: Enrolling
Updated:  8/19/2015
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
Parenting After Infant Congenital Heart Defect Diagnosis
Parenting After Infant Congenital Heart Defect Diagnosis
Status: Enrolling
Updated: 8/19/2015
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
Click here to add this to my saved trials
Study Comparing CT Scan and Stress Test in Diagnosing Coronary Artery Disease in Patients Hospitalized for Chest Pain
A Randomized Trial Comparing Multi-Detector Coronary CT Angiography and Stress Myocardial Perfusion Imaging as the Initial Test for the Diagnosis of Coronary Artery Disease in Intermediate Risk Patients Admitted for Chest Pain
Status: Enrolling
Updated:  8/21/2015
Moses Division, Montefiore Medical Center
mi
from
Bronx, NY
Study Comparing CT Scan and Stress Test in Diagnosing Coronary Artery Disease in Patients Hospitalized for Chest Pain
A Randomized Trial Comparing Multi-Detector Coronary CT Angiography and Stress Myocardial Perfusion Imaging as the Initial Test for the Diagnosis of Coronary Artery Disease in Intermediate Risk Patients Admitted for Chest Pain
Status: Enrolling
Updated: 8/21/2015
Moses Division, Montefiore Medical Center
mi
from
Bronx, NY
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Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After Percutaneous Coronary Intervention (PCI)
Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After PCI
Status: Enrolling
Updated:  8/24/2015
Methodist Hospital
mi
from
Indianapolis, IN
Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After Percutaneous Coronary Intervention (PCI)
Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After PCI
Status: Enrolling
Updated: 8/24/2015
Methodist Hospital
mi
from
Indianapolis, IN
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Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After Percutaneous Coronary Intervention (PCI)
Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After PCI
Status: Enrolling
Updated:  8/24/2015
Wishard Hospital
mi
from
Indianapolis, IN
Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After Percutaneous Coronary Intervention (PCI)
Effects of Short Term, High Dose Atorvastatin Therapy on Periprocedural Myonecrosis and Platelet Inhibition After PCI
Status: Enrolling
Updated: 8/24/2015
Wishard Hospital
mi
from
Indianapolis, IN
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
San Diego, CA
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
San Diego, CA
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Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Kansas City, KA
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Kansas City, KA
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Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Boston, MA
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Boston, MA
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Golden Valley, MN
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Golden Valley, MN
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Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
St. Louis, MO
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
St. Louis, MO
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Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
New York, NY
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
New York, NY
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Durham, NC
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Durham, NC
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Dayton, OH
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Dayton, OH
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Portland, OR
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Portland, OR
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Tualatin, OR
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Tualatin, OR
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Clinical Research Facility
mi
from
Philadelphia, PA
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Clinical Research Facility
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated:  8/27/2015
Research Site
mi
from
Altenburg,
Effect of Natalizumab on Infarct Volume in Acute Ischemic Stroke
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Safety and Efficacy of Intravenous Natalizumab (BG00002) on Reducing Infarct Volume in Acute Ischemic Stroke
Status: Enrolling
Updated: 8/27/2015
Research Site
mi
from
Altenburg,
Click here to add this to my saved trials
Pilot Study of the Feasibility of Multicenter NIRS Data Collection and Interventions for Desaturation in Cardiac Surgery
Pilot Study of the Feasibility of Multicenter NIRS Data Collection and Interventions for Desaturation in Cardiac Surgery
Status: Enrolling
Updated:  8/31/2015
Johns Hopkins Hospital
mi
from
Baltimore, MD
Pilot Study of the Feasibility of Multicenter NIRS Data Collection and Interventions for Desaturation in Cardiac Surgery
Pilot Study of the Feasibility of Multicenter NIRS Data Collection and Interventions for Desaturation in Cardiac Surgery
Status: Enrolling
Updated: 8/31/2015
Johns Hopkins Hospital
mi
from
Baltimore, MD
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The Effects Grapes on Health Indices
Pilot Study: The Effects of Whole Grapes on Markers of Health
Status: Enrolling
Updated:  9/3/2015
Ragle Human Nutrition Center
mi
from
Davis, CA
The Effects Grapes on Health Indices
Pilot Study: The Effects of Whole Grapes on Markers of Health
Status: Enrolling
Updated: 9/3/2015
Ragle Human Nutrition Center
mi
from
Davis, CA
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Pharmacogenomics of Antiplatelet Response
Pharmacogenomics of Antiplatelet Response
Status: Enrolling
Updated:  9/4/2015
Johns Hopkins School of Medicine
mi
from
Baltimore, MD
Pharmacogenomics of Antiplatelet Response
Pharmacogenomics of Antiplatelet Response
Status: Enrolling
Updated: 9/4/2015
Johns Hopkins School of Medicine
mi
from
Baltimore, MD
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Thomas Hospital
mi
from
Fairhope, AL
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Thomas Hospital
mi
from
Fairhope, AL
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Mercy Gilbert Medical Center
mi
from
Gilbert, AZ
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Mercy Gilbert Medical Center
mi
from
Gilbert, AZ
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Heart & Vascular Center of Arizona
mi
from
Phoenix, AZ
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Heart & Vascular Center of Arizona
mi
from
Phoenix, AZ
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Scottsdale Health Care
mi
from
Scottsdale, AZ
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Scottsdale Health Care
mi
from
Scottsdale, AZ
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Arkansas Heart Hospital
mi
from
Little Rock, AR
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Arkansas Heart Hospital
mi
from
Little Rock, AR
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
California Cardiovascular Consultants/ Washington Hospital
mi
from
Fremont, CA
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
California Cardiovascular Consultants/ Washington Hospital
mi
from
Fremont, CA
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Foundation for Cardiovascular Medicine
mi
from
La Jolla, CA
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Foundation for Cardiovascular Medicine
mi
from
La Jolla, CA
Click here to add this to my saved trials
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated:  9/18/2015
Mercy General Hospital
mi
from
Sacramento, CA
The Dual Antiplatelet Therapy Study (DAPT Study)
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Status: Enrolling
Updated: 9/18/2015
Mercy General Hospital
mi
from
Sacramento, CA
Click here to add this to my saved trials