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NCT02799043 · ClinicalTrials.gov registry record · NA

Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With FIRM Guided Procedures

A NA study, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
269
Enrollment target

NCT02799043: Completed NA study, sponsored by Abbott Medical Devices.

NCT02799043 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 269 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02799043, a NA study, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
269 participants
Enrollment target

Study Summary

A prospective, multicenter, randomized study to assess the safety and effectiveness of FIRM-guided procedures in conventional "redo" RF ablation procedures for the treatment of persistent and paroxysmal atrial fibrillation.

Primary Outcome

Single procedure freedom from recurrence from 3-12 months post procedure

Interventions

  • PROCEDURE FIRM-Guided Procedure and PVI
  • PROCEDURE Standard PVI

Trial Details

FieldValue
Enrollment Target 269 participants
Start Date 2016-06
Est. Completion 2020-07
Phase NA
Abbott Medical Devices

261 total trials

What the finished NCT02799043 record still lists

NCT02799043 is an interventional study that assigns participants to a tested intervention. The registered 269 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 2 interventions - of which FIRM-Guided Procedure and PVI is the first listed.

NCT02799043 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02799043 about?

NCT02799043 is a clinical study titled "Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With FIRM Guided Procedures". A prospective, multicenter, randomized study to assess the safety and effectiveness of FIRM-guided procedures in conventional "redo" RF ablation procedures for the treatment of persistent and paroxysmal atrial fibrillation.

What is the current status of trial NCT02799043?

This trial is currently completed. It is a NA study. The enrollment target is 269 participants. The study started on 2016-06. Estimated completion is 2020-07.

What interventions are being tested in trial NCT02799043?

The interventions under investigation include: FIRM-Guided Procedure and PVI (PROCEDURE), Standard PVI (PROCEDURE).

Who is sponsoring clinical trial NCT02799043?

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

How this trial's enrollment target compares

Where NCT02799043's enrollment target sits among peer trials

269 392nd of 2000 higher than 1,609 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT02799043, the US trial registry maintained by the National Library of Medicine. NCT02799043 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.