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Terminated Not applicable Interventional

Clinical Trial to Evaluate the the ReliantHeart HeartAssist 5® VAD System in Patients Awaiting Heart Transplantation

ClinicalTrials.gov ID: NCT02205411

Public ClinicalTrials.gov record NCT02205411. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:52 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Randomized, Multicenter Clinical Trial to Evaluate the Safety and Efficacy of the HeartAssist 5® VAD System Compared to the Thoratec HeartMate II® VAD and HeartWare® HVAD for Left Ventricular Support in Patients Awaiting Cardiac Transplantation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to evaluate the safety and effectiveness of the ReliantHeart HeartAssist 5® VAD System in patients listed for heart transplantation and at risk of death from refractory end-stage heart failure.

Study identification

NCT ID
NCT02205411
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
ReliantHeart Inc.
Industry
Enrollment
17 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2014 (Type not available)
Primary completion
Mar 2018 (Actual)
Completion
Mar 2018 (Actual)
Last update posted
Jul 18, 2018

2014 – 2018

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
University of California San Francisco San Francisco California 94143 —
University of Stanford Stanford California 94305 —
University of Miami Coral Gables Florida 33146 —
University of Chicago Medical Center Chicago Illinois 60637 —
Indiana University Health, Inc. d/b/a Methodist Research Institute Indianapolis Indiana 46202 —
St. Vincent Hospital & Health Care Center Indianapolis Indiana 46260 —
Jewish Hospital Louisville Kentucky 40202 —
Minneapolis Heart Institute Foundation Minneapolis Minnesota 55407 —
Mayo Clinic Hospital - Saint Mary's Campus Rochester Minnesota 55905 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
CHI St. Luke's Baylor College of Medicine Medical Center Houston Texas 77030 —
Houston Methodist Hospital Houston Texas 77030 —
University of Texas Health Science Center Houston Texas 77030 —
Providence Sacred Heart Hospital Spokane Washington 99204 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02205411, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 18, 2018 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02205411 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →