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Not listed Phase 3 Interventional

VentrAssistTM LVAD as a Bridge to Cardiac Transplantation - Pivotal Trial

ClinicalTrials.gov ID: NCT00483197

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00483197. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 15, 2026, 6:31 AM EST

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Official title

Evaluation of the VentrAssistTM Left Ventricular Assist Device as a Bridge to Cardiac Transplantation - Pivotal Trial

Brief summary

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

The purpose of this study is to evaluate the safety and effectiveness of VentrAssistTM LVAD in individuals who are awaiting heart transplants.

Study identification

NCT ID
NCT00483197
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ventracor
Industry
Enrollment
140 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
Jun 2007 (Type not available)
Primary completion
Not listed
Completion
Jun 2010 (Estimated)
Last update posted
Sep 9, 2009

2007 – 2010

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
Mayo Clinic Phoenix Arizona 85054 —
University of Florida Gainesville Florida 32610 —
Jackson Memorial Miami Florida 33136 —
Northwestern University Chicago Illinois 60611 —
Rush University Medical Center Chicago Illinois 60612 —
St. Vincent's Indianapolis Indiana 46260 —
University of Maryland School of Medicine Baltimore Maryland 21201 —
University of Minnesota Medical Center Minneapolis Minnesota 55455 —
Mayo Clinic Rochester Minnesota 55904 —
Washington University School of Medicine St Louis Missouri 63110 —
Newark Beth Israel Medical Center Newark New Jersey 07112 —
Mount Sinai Hospital New York New York 10029 —
Columbia University New York New York 10032 —
Rochester Medical Center University Rochester New York 14642 —
Montefiore Medical Center The Bronx New York 10467 —
Duke Medical Center Durham North Carolina 27710 —
Cleveland Clinic Cleveland Ohio 44195 —
Ohio State University Columbus Ohio 43210 —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Allegheny General Hospital Pittsburgh Pennsylvania 15212 —
UPMC Presbyterian Pittsburgh Pennsylvania 15213 —
Methodist Hospital Houston Texas 77030 —
University of Utah Salt Lake City Utah 84132 —
Fairfax (Inova) Hospital Falls Church Virginia 22042 —
University of Washington Seattle Washington 98185 —
Sacred Heart Medical Center Spokane Washington 99204 —
University of Wisconsin Hospital Madison Wisconsin 53792 —
St. Luke's Medical Center Milwaukee Wisconsin 53215 —

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 NCT00483197, 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 Sep 9, 2009 · Synced Nov 15, 2026

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