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NCT06676072 · ClinicalTrials.gov registry record · NA

A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PAF:

A NA study of Atrial Fibrillation (AF) and Atrial Arrhythmia, sponsored by Abbott Medical Devices.

Active
Registry status
NA
Development phase
188
Enrollment target
20
Study locations

NCT06676072: Active NA study of Atrial Fibrillation (AF) and Atrial Arrhythmia, sponsored by Abbott Medical Devices.

NCT06676072 is a NA study of Atrial Fibrillation (AF) and Atrial Arrhythmia that is active but no longer recruiting, run by Abbott Medical Devices. The registered enrollment target is 188 participants, below the 709-participant average among 17 other Atrial Fibrillation (AF) trials with a reported enrollment target (73% lower). The trial reports 20 study locations across 16 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06676072, a NA study of Atrial Fibrillation (AF) and Atrial Arrhythmia, is active but no longer recruiting, sponsored by Abbott Medical Devices.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
188 participants
Enrollment target
20
Study locations

Study Summary

The objective of this clinical study is to demonstrate that ablation with the TactiFlex SE Ablation catheter, in conjunction with a compatible pulsed field ablation (PFA) and/or radio frequency (RF) generator, is safe and effective for the treatment of symptomatic, recurrent, drug refractory paroxysmal atrial fibrillation (PAF).

Interventions

  • DEVICE PFA Ablation catheter

Study Locations (20)

Florida

  • HCA Florida Mercy Hospital - Miami
  • AdventHealth Orlando - Orlando
  • Tallahassee Research Institute - Tallahassee

Michigan

  • University of Michigan Medical Center - Ann Arbor
  • Henry Ford Providence Southfield Hospital - Southfield

New York

  • NYU Langone Health - New York
  • New York Presbyterian Hospital/Cornell University - New York

Arizona

  • HonorHealth - Scottsdale

Arkansas

  • Arkansas Heart Hospital - Little Rock

California

  • Stanford University Medical Center - Stanford

Colorado

  • South Denver Cardiology Associates PC - Littleton

Georgia

  • Piedmont Athens Regional Medical Center - Athens

Trial Details

FieldValue
Enrollment Target 188 participants
Start Date 2024-11-22
Est. Completion 2026-04-30
Phase NA
Abbott Medical Devices

261 total trials

What the registry record for NCT06676072 still lists

NCT06676072 is an interventional study that assigns participants to a tested intervention. The registered 188 participants enrollment target is mid-sized for trials with a published cap, below the 709-participant average among 17 other Atrial Fibrillation (AF) trials with a reported enrollment target (73% lower).

The record links to 4 conditions, with Atrial Fibrillation (AF) appearing as the primary indexed condition, and to 1 intervention - of which PFA Ablation catheter is the first listed.

NCT06676072 names 20 study sites across 16 states, led by Florida, Michigan, New York.

Frequently Asked Questions

What is clinical trial NCT06676072 about?

NCT06676072 is a clinical study titled "A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PAF:". The objective of this clinical study is to demonstrate that ablation with the TactiFlex SE Ablation catheter, in conjunction with a compatible pulsed field ablation (PFA) and/or radio frequency (RF) generator, is safe and effective for the treatment of symptomatic, recurrent, drug refractory paroxys...

What is the current status of trial NCT06676072?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 188 participants. The study started on 2024-11-22. Estimated completion is 2026-04-30.

What conditions does trial NCT06676072 study?

This clinical trial studies the following conditions: Atrial Fibrillation (AF), Atrial Arrhythmia, Paroxysmal AF, Drug Refractory Paroxysmal Atrial Fibrillation.

What interventions are being tested in trial NCT06676072?

The interventions under investigation include: PFA Ablation catheter (DEVICE).

Who is sponsoring clinical trial NCT06676072?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06676072 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Atrial Fibrillation (AF)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06676072's enrollment target sits among peer trials

188 14th of 17 higher than 4 of 17 other Atrial Fibrillation (AF) trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Atrial Fibrillation (AF) trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06676072, the US trial registry maintained by the National Library of Medicine. NCT06676072 (mid enrollment · wide site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.