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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 Jul 22, 2026, 10:28 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

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

Interventions

  • Clinical Management Recommendations for reducing pump thrombosis Other

Other

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
Aug 31, 2014
Primary completion
Feb 29, 2016
Completion
May 31, 2016
Last update posted
Mar 24, 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 24, 2022 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02158403 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →