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Terminated No phase listed Observational

TandemHeart Experiences and MEthods (THEME Registry)

ClinicalTrials.gov ID: NCT02326402

Public ClinicalTrials.gov record NCT02326402. 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 21, 2026, 12:17 PM EDT

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

Official title

THEME Registry: TandemHeart Experiences and MEthods (THEME Registry)

Brief summary

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

This study is intended to be a multicenter, prospective observation registry. By collecting prospective descriptive data, provide insight into disease defining characteristics resulting in the clinical decision to use TandemHeart® or LifeSPARC™ System for mechanical support and enhance knowledge of best practice regarding clinical management, weaning and removal/exit strategies.

Study identification

NCT ID
NCT02326402
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
CardiacAssist, Inc.
Industry
Enrollment
365 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
Dec 2014 (Actual)
Primary completion
Dec 2022 (Actual)
Completion
Jan 2023 (Actual)
Last update posted
Sep 21, 2023

2014 – 2023

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Princeton-Baptist Medical Center Birmingham Alabama 35233 —
Banner - University Medical Center Tucson Tucson Arizona 85724 —
University of California, San Diego La Jolla California 92037 —
Cedars-Sinai Medical Center Los Angeles California 90048 —
St. John's Hospital Springfield Illinois 62769 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
University of Michigan Health System Ann Arbor Michigan 48109 —
Henry Ford Hospital Detroit Michigan 48202 —
St. Louis University Hospital St Louis Missouri 63110 —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Temple University Hospital Philadelphia Pennsylvania 19140 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
University of Virginia Health System Charlottesville Virginia 22908 —
Providence Sacred Heart Medical Center & Children's Hospital Spokane Washington 99204 —
Medical College of Wisconsin-Froedtert Hospital Milwaukee Wisconsin 53226 —

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 NCT02326402, 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 21, 2023 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02326402 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →