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Terminated Not applicable Interventional

Posterior Wall Substrate Modification Using Irreversible Electroporation for Paroxysmal Atrial Fibrillation

ClinicalTrials.gov ID: NCT06364215

Public ClinicalTrials.gov record NCT06364215. 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 May 20, 2026, 2:10 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

Posterior Wall Substrate Modification Using Irreversible Electroporation for the Treatment of Paroxysmal Atrial Fibrillation

Study identification

NCT ID
NCT06364215
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Jorge Romero
Other
Enrollment
198 participants

Conditions and interventions

Interventions

  • Farapulse PFA, Pulmonary Vein Isolation alone Device
  • Farapulse PFA, Pulmonary Vein Isolation and Left atrial Posterior Wall Isolation Device

Device

Eligibility (public fields only)

Age range
21 Years to 90 Years
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
Oct 7, 2024
Primary completion
Nov 15, 2025
Completion
Nov 15, 2025
Last update posted
May 14, 2026

2024 – 2025

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Grandview Medical Center Birmingham Alabama 35243
MedStar Washington Hospital Center Washington D.C. District of Columbia 20010
St. Vincent's Health System, Inc. d/b/a Ascension St. Vincent's Jacksonville Florida 32204
HCA Florida Mercy Hospital Miami Florida 33133
St. Luke's Boise Medical Center Boise Idaho 83712
Maine Medical Center Portland Maine 04102
Brigham and Women's Hospital Boston Massachusetts 02115
Lahey Hospital and Medical Center Burlington Massachusetts 01805
Corewell Health William Beaumont Hospital Royal Oak Michigan 48073
The Valley Hospital Paramus New Jersey 07652
North Shore University Hospital, Northwell Health Manhasset New York 11030
Doylestown Hospital Doylestown Pennsylvania 18901
Trident Medical Center Charleston South Carolina 29406
Medical University of South Carolina Charleston South Carolina 29425
Orion Medical Houston Texas 77034
Methodist Hospital-San Antonio San Antonio Texas 78229
University of Texas Health Science Center at San Antonio San Antonio Texas 78229
University of Washington Medical Center Seattle Washington 98195

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 NCT06364215, 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 May 14, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06364215 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →