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Active, not recruiting No phase listed Observational

Abbott Atrial Fibrillation Post Approval Study

ClinicalTrials.gov ID: NCT05434650

Public ClinicalTrials.gov record NCT05434650. 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 23, 2026, 4:42 PM EDT

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

Brief summary

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

This post-approval study is designed to provide continued real-world clinical evidence to confirm the safety and long-term effectiveness of atrial fibrillation (AF) radiofrequency (RF) technologies (e.g. TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™ (TactiCath SE)) for the treatment of AF.

Study identification

NCT ID
NCT05434650
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Abbott Medical Devices
Industry
Enrollment
200 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 21, 2022 (Actual)
Primary completion
Oct 22, 2024 (Actual)
Completion
Nov 30, 2026 (Estimated)
Last update posted
Nov 19, 2025

2022 – 2026

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Heart Center Research, LLC. Huntsville Alabama 35801 —
Arkansas Cardiology Little Rock Arkansas 72205 —
Eisenhower Medical Center Rancho Mirage California 92270 —
Sequoia Hospital Redwood City California 94062 —
Northside Hospital Atlanta Georgia 30342 —
Ochsner Medical Center New Orleans Louisiana 70121 —
Brigham & Women's Hospital Boston Massachusetts 02115 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Providence Hospital Southfield Michigan 48075 —
North Mississippi Medical Center Tupelo Mississippi 38801 —
St. Patrick Hospital Missoula Montana 59802 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
Oklahoma Heart Hospital South Oklahoma City Oklahoma 73135 —
Doylestown Hospital Doylestown Pennsylvania 18901 —
Erlanger Medical Center Chattanooga Tennessee 37403 —
Centennial Medical Center Nashville Tennessee 37203 —
Methodist Hospital of San Antonio San Antonio Texas 78229 —
St. Marks Hospital Salt Lake City Utah 84124 —
Sentara Norfolk General Hospital Norfolk Virginia 23507 —
Chippenham Hospital Richmond Virginia 23225 —

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 NCT05434650, 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 19, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05434650 live on ClinicalTrials.gov.

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