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Completed Not applicable Interventional

PREVENtion of HeartMate II Pump Thrombosis

ClinicalTrials.gov ID: NCT02158403

Public ClinicalTrials.gov record NCT02158403. 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 26, 2026, 6:56 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

PREVENtion of HeartMate II Pump Thrombosis Through Clinical Management

Brief summary

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

The purpose of this study is to assess how often blood clots form in the FDA-approved HeartMate® II (HM II) Left Ventricular Assist Device (LVAD) and to identify risks related to clotting within the pump.

Study identification

NCT ID
NCT02158403
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Abbott Medical Devices
Industry
Enrollment
300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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 2016 (Actual)
Completion
Jun 2016 (Actual)
Last update posted
Mar 25, 2022

2014 – 2016

United States locations

U.S. sites
23
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Baptist Medical Center Little Rock Arkansas 72205 —
University of California, San Diego La Jolla California 92037 —
UCLA Medical Center Los Angeles California 90095 —
Sutter Memorial Sacramento California 95819 —
Sharp Memorial Hospital San Diego California 92123 —
University of Colorado Aurora Colorado 80045 —
Shands Hospital at University of Florida Gainesville Florida 32610 —
Northwestern Memorial Chicago Illinois 60611 —
University of Chicago Chicago Illinois 60637 —
Jewish Hospital Louisville Kentucky 40202 —
Abbott Northwestern Minneapolis Minnesota 55407 —
University of Minnesota Medical Center Minneapolis Minnesota 55455 —
Mayo Clinic, St. Mary's Rochester Minnesota 55905 —
University of North Carolina Chapel Hill North Carolina 27599 —
The Christ Hospital Cincinnati Ohio 45219 —
Ohio State University Columbus Ohio 43210 —
Abington Memorial Hospital Abington Pennsylvania 19001 —
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107 —
Allegheny General Hospital Pittsburgh Pennsylvania 15212 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
Memorial Hermann/UT Texas Houston Texas 77030 —
Inova Fairfax Hospital Falls Church Virginia 22042 —

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 NCT02158403, 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 Mar 25, 2022 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02158403 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →