The PIVATAL Study -Study of Ventricular Arrhythmia (VTA) Ablation in Left Ventricular Assist Device (LVAD) Patients

ClinicalTrials.gov ID: NCT05034432

Public ClinicalTrials.gov record NCT05034432. 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.

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ClinicalTrials.gov public records Last synced Sep 2, 2026, 3:51 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

Prophylactic Intra-Operative Ventricular Arrhythmia Ablation in High-Risk LVAD Candidates (PIVATAL)

Brief summary

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

To investigate the effect of VTA ablation at the time of LVAD implant to see if it can reduce the incidence of VTA after surgery

Study identification

NCT ID: NCT05034432
Recruitment status: Recruiting
Study type: Interventional
Phase: Phase 4
Lead sponsor: University of Rochester; Other
Enrollment: 100 participants

Conditions and interventions

Conditions

Interventions

Intra-Op Prophylactic VT ablation Procedure
Conventional Management Other

Procedure · Other

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: May 26, 2022
Primary completion: Apr 29, 2027
Completion: Jun 29, 2027
Last update posted: Jul 13, 2026

2022 – 2027

United States locations

U.S. sites: 19
U.S. states: 15
U.S. cities: 18

Facility	City	State	ZIP	Site status
Banner University Medical Center	Phoenix	Arizona	85006	Recruiting
UCLA Cardiac Arrthmia Center	Los Angeles	California	90095	Recruiting
University of California San Francisco	San Francisco	California	94143	Recruiting
Medstar Washington Hospital Center	Washington D.C.	District of Columbia	20010	Recruiting
Piedmont Heart Institute	Atlanta	Georgia	30309	Recruiting
Emory University	Atlanta	Georgia	30322	Recruiting
Ascension St. Vincent Indianapolis	Indianapolis	Indiana	46260	Recruiting
Univedrsity of Louisville	Louisville	Kentucky	40202	Recruiting
Johns Hopkins University	Baltimore	Maryland	21287	Recruiting
Tufts Medical Center	Boston	Massachusetts	02111	Recruiting
Henry Ford Health	Detroit	Michigan	48202	Recruiting
Columbia University Medical Center	New York	New York	10026	Recruiting
University of Rochester	Rochester	New York	14642	Recruiting
Cleveland Clinic	Cleveland	Ohio	44195	Recruiting
University of Pennsylvania	Philadelphia	Pennsylvania	19104	Recruiting
UPMC	Pittsburgh	Pennsylvania	15213	Recruiting
Medical University of South Carolina	Charleston	South Carolina	29425	Recruiting
Vanderbilt University Medical Center	Nashville	Tennessee	37232	Recruiting
Houston Methodist Hospital	Houston	Texas	77030	Recruiting

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 NCT05034432, 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 Jul 13, 2026 · Synced Sep 2, 2026

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The complete protocol, eligibility criteria, and contact information for NCT05034432 live on ClinicalTrials.gov.

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