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Active, not recruiting Not applicable Interventional

CONVERGE Post-Approval Study (PAS)

ClinicalTrials.gov ID: NCT05393180

Public ClinicalTrials.gov record NCT05393180. 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 Nov 6, 2026, 1:48 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Hybrid Convergent of Epicardial and Endocardial RF Ablation for the Treatment of Symptomatic Longstanding Persistent AF

Brief summary

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

The primary objective of CONVERGE PAS is to evaluate clinical outcomes (peri-procedural and long-term) in a cohort of patients treated during commercial use of the EPi-Sense® Guided Coagulation System or EPi-Sense ST™ Coagulation System to treat symptomatic long-standing persistent atrial fibrillation (AF) patients who are refractory or intolerant to at least one Class I and/or III AAD.

Study identification

NCT ID
NCT05393180
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
AtriCure, Inc.
Industry
Enrollment
53 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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
Apr 13, 2022 (Actual)
Primary completion
Feb 26, 2027 (Estimated)
Completion
Nov 21, 2028 (Estimated)
Last update posted
Nov 6, 2026

2022 – 2028

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Sutter Bay Hospitals San Francisco California 94107 —
Hartford Hospital Hartford Connecticut 06102 —
Baycare Health Systems Clearwater Florida 33759 —
Orlando Health Orlando Florida 32806 —
Emory Saint Joseph Hopsital Atlanta Georgia 30322 —
Wellstar Health System Marietta Georgia 30062 —
Norton Heart & Vascular Institute Louisville Kentucky 40205 —
MedStar Union Memorial Hospital Baltimore Maryland 21218 —
Southcoast Hospitals Group New Bedford Massachusetts 02740 —
AtlantiCare Medical Center Atlantic City New Jersey 08401 —
Avera Heart Hospital of SD Sioux Falls South Dakota 57108 —
University of Utah Salt Lake City Utah 84112 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05393180, 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 Nov 6, 2026 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05393180 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →