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
1504
mi
from 98109
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
1504
mi
from 98109
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
2400
mi
from 98109
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
2400
mi
from 98109
New York City, 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
Lenox Hill Hospital
2402
mi
from 98109
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
2402
mi
from 98109
New York, 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
University of Toledo
1927
mi
from 98109
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
1927
mi
from 98109
Toledo, OH
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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
Temple University Hospital
2373
mi
from 98109
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
2373
mi
from 98109
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
1740
mi
from 98109
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
1740
mi
from 98109
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
2457
mi
from 98109
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
2457
mi
from 98109
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
2547
mi
from 98109
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
2547
mi
from 98109
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
2178
mi
from 98109
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
2178
mi
from 98109
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
2281
mi
from 98109
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
2281
mi
from 98109
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
2484
mi
from 98109
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
2484
mi
from 98109
Boston, MA
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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
2432
mi
from 98109
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
2432
mi
from 98109
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
1868
mi
from 98109
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
1868
mi
from 98109
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
2328
mi
from 98109
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
2328
mi
from 98109
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
2134
mi
from 98109
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
2134
mi
from 98109
Pittsburgh, PA
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Interactive Cholesterol Advisory Tool
The Interactive Cholesterol Advisory Tool
Status: Enrolling
Updated:  8/5/2015
University of Rochester
2161
mi
from 98109
Rochester, NY
Interactive Cholesterol Advisory Tool
The Interactive Cholesterol Advisory Tool
Status: Enrolling
Updated: 8/5/2015
University of Rochester
2161
mi
from 98109
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
680
mi
from 98109
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
680
mi
from 98109
San Francisco, CA
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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
682
mi
from 98109
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
682
mi
from 98109
San Francisco, CA
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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
2220
mi
from 98109
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
2220
mi
from 98109
Hershey, PA
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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
1780
mi
from 98109
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
1780
mi
from 98109
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
2145
mi
from 98109
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
2145
mi
from 98109
Mobile, AL
Click here to add this to my saved trials
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
1898
mi
from 98109
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
1898
mi
from 98109
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
1616
mi
from 98109
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
1616
mi
from 98109
Madison, WI
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
Children's Hospital of Wisconsin
1681
mi
from 98109
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
1681
mi
from 98109
Milwaukee, WI
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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
2403
mi
from 98109
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
2403
mi
from 98109
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
1867
mi
from 98109
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
1867
mi
from 98109
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
1867
mi
from 98109
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
1867
mi
from 98109
Indianapolis, IN
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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
1065
mi
from 98109
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
1065
mi
from 98109
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
1500
mi
from 98109
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
1500
mi
from 98109
Kansas City, KA
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
2485
mi
from 98109
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
2485
mi
from 98109
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
1386
mi
from 98109
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
1386
mi
from 98109
Golden Valley, MN
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
1720
mi
from 98109
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
1720
mi
from 98109
St. Louis, MO
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
2400
mi
from 98109
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
2400
mi
from 98109
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
2341
mi
from 98109
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
2341
mi
from 98109
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
1961
mi
from 98109
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
1961
mi
from 98109
Dayton, OH
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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
147
mi
from 98109
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
147
mi
from 98109
Portland, OR
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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
156
mi
from 98109
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
156
mi
from 98109
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
2373
mi
from 98109
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
2373
mi
from 98109
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
5113
mi
from 98109
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
5113
mi
from 98109
Altenburg,
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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
2329
mi
from 98109
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
2329
mi
from 98109
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
628
mi
from 98109
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
628
mi
from 98109
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
2329
mi
from 98109
Baltimore, MD
Pharmacogenomics of Antiplatelet Response
Pharmacogenomics of Antiplatelet Response
Status: Enrolling
Updated: 9/4/2015
Johns Hopkins School of Medicine
2329
mi
from 98109
Baltimore, MD
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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
2167
mi
from 98109
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
2167
mi
from 98109
Fairhope, AL
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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
1136
mi
from 98109
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
1136
mi
from 98109
Gilbert, AZ
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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
1115
mi
from 98109
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
1115
mi
from 98109
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
1113
mi
from 98109
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
1113
mi
from 98109
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
1776
mi
from 98109
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
1776
mi
from 98109
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
698
mi
from 98109
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
698
mi
from 98109
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
1056
mi
from 98109
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
1056
mi
from 98109
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
627
mi
from 98109
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
627
mi
from 98109
Sacramento, CA
Click here to add this to my saved trials