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Completed No phase listed Observational

Driveline Silicone Skin Interface Registry

ClinicalTrials.gov ID: NCT01577433

Public ClinicalTrials.gov record NCT01577433. 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 Sep 5, 2026, 2:32 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

Driveline Silicone Skin Interface (SSI) Registry

Brief summary

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

The purpose of this observational registry is to determine the freedom from driveline (DL) infection events in subjects implanted with a HeartMate II LVAD in whom only the silicone portion of the DL is externalized resulting in a silicone skin interface (SSI)

Study identification

NCT ID
NCT01577433
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Abbott Medical Devices
Industry
Enrollment
400 participants

Conditions and interventions

Interventions

Not listed

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
Apr 30, 2012
Primary completion
Jun 30, 2018
Completion
Nov 30, 2018
Last update posted
Mar 12, 2019

2012 – 2018

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
Yale New Haven Hospital New Haven Connecticut 06520
Tampa General Hospital Tampa Florida 33606
Piedmont Heart Institute Atlanta Georgia 30309
University of Chicago Medical Center Chicago Illinois 60637
Advocate Christ Medical Center Oak Lawn Illinois 60453
St.Vincent's Hospital and Health Services Indianapolis Indiana 46260
University of Iowa Hospital Iowa City Iowa 52242
Henry Ford Hospital Detroit Michigan 48202
Abbott Northwestern Minneapolis Minnesota 55407
Washington University - Barnes Jewish Hospital St Louis Missouri 63110
University of North Carolina Chapel Hill North Carolina 27599
Baylor Medical Center Dallas Texas 75226
Intermountain Medical Center Murray Utah 84107
Virginia Commonwealth University Richmond Virginia 23298
Sacred Heart Medical Center 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 NCT01577433, 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 12, 2019 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01577433 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →