Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
31,654
archived clinical trials in
Cardiology

The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
U.T. Southwestern Medical Center
mi
from
Dallas, TX
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
U.T. Southwestern Medical Center
mi
from
Dallas, TX
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The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
Baylor College of Medicine
mi
from
Houston, TX
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
Baylor College of Medicine
mi
from
Houston, TX
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The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
Wilford Hall Medical Center
mi
from
Lackland Air Force Base, TX
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
Wilford Hall Medical Center
mi
from
Lackland Air Force Base, TX
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The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
Texas
mi
from
Temple, TX
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
Texas
mi
from
Temple, TX
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The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
University of Virginia
mi
from
Charlottesville, VA
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
University of Virginia
mi
from
Charlottesville, VA
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The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
Sentara Heart Hospital
mi
from
Norfolk, VA
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
Sentara Heart Hospital
mi
from
Norfolk, VA
Click here to add this to my saved trials
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
Sacred Heart Medical Center
mi
from
Spokane, WA
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
Sacred Heart Medical Center
mi
from
Spokane, WA
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The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated:  12/31/1969
Wisconsin Heart / Meriter Hospital
mi
from
Madison, WI
The (PIVOTAL) Study
Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL)
Status: Enrolling
Updated: 12/31/1969
Wisconsin Heart / Meriter Hospital
mi
from
Madison, WI
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The Healthy Heart Study
Improving Delivery of Patient-Centered Cardiac Rehabilitation
Status: Enrolling
Updated:  12/31/1969
San Francisco Veterans Affairs Medical Center
mi
from
San Francisco, CA
The Healthy Heart Study
Improving Delivery of Patient-Centered Cardiac Rehabilitation
Status: Enrolling
Updated: 12/31/1969
San Francisco Veterans Affairs Medical Center
mi
from
San Francisco, CA
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Effectiveness of Sorbion in the Treatment of Venous Leg Ulcers The Protocol Elements
Effectiveness of Sorbion in the Treatment of Venous Leg Ulcers The Protocol Elements
Status: Enrolling
Updated:  12/31/1969
University of Toledo Medical Center
mi
from
Toledo, OH
Effectiveness of Sorbion in the Treatment of Venous Leg Ulcers The Protocol Elements
Effectiveness of Sorbion in the Treatment of Venous Leg Ulcers The Protocol Elements
Status: Enrolling
Updated: 12/31/1969
University of Toledo Medical Center
mi
from
Toledo, OH
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Pilot Study of Pre-Ischemic Conditioning for Intracranial Atherosclerosis
Pilot Study of Pre-Ischemic Conditioning for Intracranial Atherosclerosis
Status: Enrolling
Updated:  12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
Pilot Study of Pre-Ischemic Conditioning for Intracranial Atherosclerosis
Pilot Study of Pre-Ischemic Conditioning for Intracranial Atherosclerosis
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
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Effectiveness of Oral Anticoagulants in Elderly Patients With Non-Valvular Atrial Fibrillation and Heart Failure
Real-World Comparative Effectiveness Research Among Elderly Non-valvular Atrial Fibrillation (NVAF) Patients With Heart Failure (HF) Using Oral Anticoagulants
Status: Enrolling
Updated:  12/31/1969
Local Institution
mi
from
Ann Arbor, MI
Effectiveness of Oral Anticoagulants in Elderly Patients With Non-Valvular Atrial Fibrillation and Heart Failure
Real-World Comparative Effectiveness Research Among Elderly Non-valvular Atrial Fibrillation (NVAF) Patients With Heart Failure (HF) Using Oral Anticoagulants
Status: Enrolling
Updated: 12/31/1969
Local Institution
mi
from
Ann Arbor, MI
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Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated:  12/31/1969
Orlando Health
mi
from
Orlando, FL
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated: 12/31/1969
Orlando Health
mi
from
Orlando, FL
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Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated:  12/31/1969
Prairie Heart
mi
from
Springfield, IL
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated: 12/31/1969
Prairie Heart
mi
from
Springfield, IL
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Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated:  12/31/1969
Metro Health Hospital
mi
from
Wyoming, MI
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated: 12/31/1969
Metro Health Hospital
mi
from
Wyoming, MI
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Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated:  12/31/1969
Cox Health
mi
from
Springfield, MO
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated: 12/31/1969
Cox Health
mi
from
Springfield, MO
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Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated:  12/31/1969
Rex Healthcare
mi
from
Raleigh, NC
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated: 12/31/1969
Rex Healthcare
mi
from
Raleigh, NC
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Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated:  12/31/1969
The Hospitals of Providence
mi
from
El Paso, TX
Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"
Peripheral Registry of Endovascular Clinical Outcomes
Status: Enrolling
Updated: 12/31/1969
The Hospitals of Providence
mi
from
El Paso, TX
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Ischemic Preconditioning Claudication Study
Walking Capacity of Patients With Claudication in Lower Extremities Following Ischemic Preconditioning
Status: Enrolling
Updated:  12/31/1969
Froedtert and the Medical College of Wisconsin
mi
from
Milwaukee, WI
Ischemic Preconditioning Claudication Study
Walking Capacity of Patients With Claudication in Lower Extremities Following Ischemic Preconditioning
Status: Enrolling
Updated: 12/31/1969
Froedtert and the Medical College of Wisconsin
mi
from
Milwaukee, WI
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Phase 1 Clinical Trial of Sodium Nitrite for Out of Hospital Cardiac Arrest
Phase 1 Clinical Trial of Sodium Nitrite for Out of Hospital Cardiac Arrest
Status: Enrolling
Updated:  12/31/1969
Univ of Washington
mi
from
Seattle, WA
Phase 1 Clinical Trial of Sodium Nitrite for Out of Hospital Cardiac Arrest
Phase 1 Clinical Trial of Sodium Nitrite for Out of Hospital Cardiac Arrest
Status: Enrolling
Updated: 12/31/1969
Univ of Washington
mi
from
Seattle, WA
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BVS-OCT Imaging Study
Bioabsorbable Drug-eluting Scaffolds (BVS)-Optical Coherence Tomography (OCT) Imaging Study
Status: Enrolling
Updated:  12/31/1969
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
BVS-OCT Imaging Study
Bioabsorbable Drug-eluting Scaffolds (BVS)-Optical Coherence Tomography (OCT) Imaging Study
Status: Enrolling
Updated: 12/31/1969
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
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Heart Failure Hospital Readmissions and Physical Therapy
Investigating All-Cause 30-Day Hospital Readmisisons in Patients Discharged From a Tertiary Teaching Hospital With Acute Decompensated Heart Failure Diagnosis
Status: Enrolling
Updated:  12/31/1969
Houston Methodist Hospital
mi
from
Houston, TX
Heart Failure Hospital Readmissions and Physical Therapy
Investigating All-Cause 30-Day Hospital Readmisisons in Patients Discharged From a Tertiary Teaching Hospital With Acute Decompensated Heart Failure Diagnosis
Status: Enrolling
Updated: 12/31/1969
Houston Methodist Hospital
mi
from
Houston, TX
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Efficacy and Safety of HMR1766 in Patients With Fontaine Stage II Peripheral Arterial Disease
A Randomized, Double-blind, Placebo-controlled, Parallel Group Trial of HMR1766 Assessing the Efficacy and Safety of 3 Doses of HMR1766 Versus Placebo With Cilostazol as a Calibrator, Administered for 26 Weeks in Patients With Peripheral Arterial Disease (PAD) Fontaine Stage II
Status: Enrolling
Updated:  12/31/1969
Sanofi-Aventis Administrative Office
mi
from
Bridgewater, NJ
Efficacy and Safety of HMR1766 in Patients With Fontaine Stage II Peripheral Arterial Disease
A Randomized, Double-blind, Placebo-controlled, Parallel Group Trial of HMR1766 Assessing the Efficacy and Safety of 3 Doses of HMR1766 Versus Placebo With Cilostazol as a Calibrator, Administered for 26 Weeks in Patients With Peripheral Arterial Disease (PAD) Fontaine Stage II
Status: Enrolling
Updated: 12/31/1969
Sanofi-Aventis Administrative Office
mi
from
Bridgewater, NJ
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Efficacy and Safety of HMR1766 in Patients With Fontaine Stage II Peripheral Arterial Disease
A Randomized, Double-blind, Placebo-controlled, Parallel Group Trial of HMR1766 Assessing the Efficacy and Safety of 3 Doses of HMR1766 Versus Placebo With Cilostazol as a Calibrator, Administered for 26 Weeks in Patients With Peripheral Arterial Disease (PAD) Fontaine Stage II
Status: Enrolling
Updated:  12/31/1969
Sanofi-Aventis Administrative Office
mi
from
Vienna,
Efficacy and Safety of HMR1766 in Patients With Fontaine Stage II Peripheral Arterial Disease
A Randomized, Double-blind, Placebo-controlled, Parallel Group Trial of HMR1766 Assessing the Efficacy and Safety of 3 Doses of HMR1766 Versus Placebo With Cilostazol as a Calibrator, Administered for 26 Weeks in Patients With Peripheral Arterial Disease (PAD) Fontaine Stage II
Status: Enrolling
Updated: 12/31/1969
Sanofi-Aventis Administrative Office
mi
from
Vienna,
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Value of Genetic Counseling and Testing for Patients Who Would Like to Know More About Their Personal Risk of AMD
Value of Genetic Counseling and Testing for Patients Who Would Like to Know More About Their Personal Risk of AMD
Status: Enrolling
Updated:  12/31/1969
University of Utah, John A. Moran Eye Center
mi
from
Salt Lake City, UT
Value of Genetic Counseling and Testing for Patients Who Would Like to Know More About Their Personal Risk of AMD
Value of Genetic Counseling and Testing for Patients Who Would Like to Know More About Their Personal Risk of AMD
Status: Enrolling
Updated: 12/31/1969
University of Utah, John A. Moran Eye Center
mi
from
Salt Lake City, UT
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Comprehensive Medication Monitoring on Heart Failure Patient Outcomes
A Pilot Prospective, Randomized Controlled Trial Assessing the Impact of Clinical Decision Support Using Comprehensive Medication Monitoring on Heart Failure Patient Outcomes
Status: Enrolling
Updated:  12/31/1969
UPMC Heart & Vascular Institute
mi
from
Pittsburgh, PA
Comprehensive Medication Monitoring on Heart Failure Patient Outcomes
A Pilot Prospective, Randomized Controlled Trial Assessing the Impact of Clinical Decision Support Using Comprehensive Medication Monitoring on Heart Failure Patient Outcomes
Status: Enrolling
Updated: 12/31/1969
UPMC Heart & Vascular Institute
mi
from
Pittsburgh, PA
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Angiotensin (1-7) Treatment to Improve Cognitive Functioning in Heart Failure Patients
Angiotensin (1-7) Treatment to Improve Cognitive Functioning in Heart Failure Patients
Status: Enrolling
Updated:  12/31/1969
The University of Arizona Sarver Heart Center
mi
from
Tucson, AZ
Angiotensin (1-7) Treatment to Improve Cognitive Functioning in Heart Failure Patients
Angiotensin (1-7) Treatment to Improve Cognitive Functioning in Heart Failure Patients
Status: Enrolling
Updated: 12/31/1969
The University of Arizona Sarver Heart Center
mi
from
Tucson, AZ
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Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated:  12/31/1969
Oregon Health and Science University
mi
from
Portland, OR
Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated: 12/31/1969
Oregon Health and Science University
mi
from
Portland, OR
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Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated:  12/31/1969
Yale-New Haven Hospital
mi
from
New Haven, CT
Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated: 12/31/1969
Yale-New Haven Hospital
mi
from
New Haven, CT
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Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated:  12/31/1969
Mayo Clinic Arizona, Mayo Clinic Scottsdale
mi
from
Scottsdale, AZ
Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Arizona, Mayo Clinic Scottsdale
mi
from
Scottsdale, AZ
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Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated:  12/31/1969
Duke Cardiology at Southpoint
mi
from
Durham, NC
Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in PIONEER
An Open-Label Extension Study of Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Previously Enrolled in Study MYK-461-004 (PIONEER)
Status: Enrolling
Updated: 12/31/1969
Duke Cardiology at Southpoint
mi
from
Durham, NC
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A Study to Compare the Risk of a Major Bleeding in Participants Who Received Blood Thinning Medications Following a Blood Clot
Risk of Major Bleeding Associated With Apixaban Verses Warfarin in the Treatment of Venous Thromboembolism in US Clinical Practice
Status: Enrolling
Updated:  12/31/1969
Local Institution
mi
from
Princeton, NJ
A Study to Compare the Risk of a Major Bleeding in Participants Who Received Blood Thinning Medications Following a Blood Clot
Risk of Major Bleeding Associated With Apixaban Verses Warfarin in the Treatment of Venous Thromboembolism in US Clinical Practice
Status: Enrolling
Updated: 12/31/1969
Local Institution
mi
from
Princeton, NJ
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Alirocumab and Reverse Cholesterol Transport
Effect of Alirocumab on Reverse Cholesterol Transport in Humans
Status: Enrolling
Updated:  12/31/1969
Washington University School of Medicine
mi
from
Saint Louis, MO
Alirocumab and Reverse Cholesterol Transport
Effect of Alirocumab on Reverse Cholesterol Transport in Humans
Status: Enrolling
Updated: 12/31/1969
Washington University School of Medicine
mi
from
Saint Louis, MO
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Safety and Tolerability Study of E-WE Thrombin in Healthy Adult Subjects
A Phase 1, Single Ascending Dose, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of E-WE Thrombin as an Intravenous Bolus in Healthy Adult Subjects
Status: Enrolling
Updated:  12/31/1969
Celerion
mi
from
Tempe, AZ
Safety and Tolerability Study of E-WE Thrombin in Healthy Adult Subjects
A Phase 1, Single Ascending Dose, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of E-WE Thrombin as an Intravenous Bolus in Healthy Adult Subjects
Status: Enrolling
Updated: 12/31/1969
Celerion
mi
from
Tempe, AZ
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Use of Non-Invasive Positive Pressure Ventilation in Patients With Severe Obesity Undergoing Upper Endoscopy Procedures
Use of Non-Invasive Positive Pressure Ventilation in Patients With Severe Obesity Undergoing Upper Endoscopy Procedures
Status: Enrolling
Updated:  12/31/1969
Bristol Hospital
mi
from
Bristol, CT
Use of Non-Invasive Positive Pressure Ventilation in Patients With Severe Obesity Undergoing Upper Endoscopy Procedures
Use of Non-Invasive Positive Pressure Ventilation in Patients With Severe Obesity Undergoing Upper Endoscopy Procedures
Status: Enrolling
Updated: 12/31/1969
Bristol Hospital
mi
from
Bristol, CT
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Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD)
Comparison of Ventricular Fibrillation Induction Techniques During Medtronic Implantable Cardioverter Defibrillator Implant
Status: Enrolling
Updated:  12/31/1969
Wellmont CVA Heart Institute
mi
from
Kingsport, TN
Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD)
Comparison of Ventricular Fibrillation Induction Techniques During Medtronic Implantable Cardioverter Defibrillator Implant
Status: Enrolling
Updated: 12/31/1969
Wellmont CVA Heart Institute
mi
from
Kingsport, TN
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ENABLE CHF-PC (Comprehensive Heartcare For Patients and Caregivers)
Randomized Trial of ENABLE CHF-PC for Heart Failure Patients and Caregivers. (Comprehensive Heartcare For Patients and Caregivers)
Status: Enrolling
Updated:  12/31/1969
Birmingham Veterans Affairs Medical Center (BVAMC)
mi
from
Birmingham, AL
ENABLE CHF-PC (Comprehensive Heartcare For Patients and Caregivers)
Randomized Trial of ENABLE CHF-PC for Heart Failure Patients and Caregivers. (Comprehensive Heartcare For Patients and Caregivers)
Status: Enrolling
Updated: 12/31/1969
Birmingham Veterans Affairs Medical Center (BVAMC)
mi
from
Birmingham, AL
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ENABLE CHF-PC (Comprehensive Heartcare For Patients and Caregivers)
Randomized Trial of ENABLE CHF-PC for Heart Failure Patients and Caregivers. (Comprehensive Heartcare For Patients and Caregivers)
Status: Enrolling
Updated:  12/31/1969
University of Alabama at Birmingham, School of Nursing, Dept. Acute, Chronic and Continuing Care
mi
from
Birmingham, AL
ENABLE CHF-PC (Comprehensive Heartcare For Patients and Caregivers)
Randomized Trial of ENABLE CHF-PC for Heart Failure Patients and Caregivers. (Comprehensive Heartcare For Patients and Caregivers)
Status: Enrolling
Updated: 12/31/1969
University of Alabama at Birmingham, School of Nursing, Dept. Acute, Chronic and Continuing Care
mi
from
Birmingham, AL
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Hemodynamic Assessment in Acute Decompensated Heart Failure
Hemodynamic Assessment Throughout Diuretic Treatment in Acute Decompensated Heart Failure
Status: Enrolling
Updated:  12/31/1969
New Mexico Heart Institute
mi
from
Albuquerque, NM
Hemodynamic Assessment in Acute Decompensated Heart Failure
Hemodynamic Assessment Throughout Diuretic Treatment in Acute Decompensated Heart Failure
Status: Enrolling
Updated: 12/31/1969
New Mexico Heart Institute
mi
from
Albuquerque, NM
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Hemodynamic Assessment in Acute Decompensated Heart Failure
Hemodynamic Assessment Throughout Diuretic Treatment in Acute Decompensated Heart Failure
Status: Enrolling
Updated:  12/31/1969
University Hospital of Split
mi
from
Split,
Hemodynamic Assessment in Acute Decompensated Heart Failure
Hemodynamic Assessment Throughout Diuretic Treatment in Acute Decompensated Heart Failure
Status: Enrolling
Updated: 12/31/1969
University Hospital of Split
mi
from
Split,
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Yuma, AZ
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Yuma, AZ
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Fayetteville, AR
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Fayetteville, AR
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Fort Smith, AR
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Fort Smith, AR
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Bakersfield, CA
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Bakersfield, CA
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Berkeley, CA
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Berkeley, CA
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Los Angeles, CA
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Los Angeles, CA
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Aurora, CO
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Aurora, CO
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Stamford, CT
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Stamford, CT
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Clearwater, FL
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Clearwater, FL
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Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Daytona Beach, FL
Study for Atrial Fibrillation Reduction (SAFARI)
Study for Atrial Fibrillation Reduction (SAFARI)
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Daytona Beach, FL
Click here to add this to my saved trials