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NCT04190186 · ClinicalTrials.gov registry record · NA

Hybrid Ablation Plus Medical Therapy for Persistent Atrial Fibrillation

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
55
Enrollment target

NCT04190186: Completed NA study, sponsored by University of Rochester.

NCT04190186 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 55 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04190186, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
55 participants
Enrollment target

Study Summary

This clinical trial is designed to compare two management strategies for the treatment of asymptomatic/subclinical atrial fibrillation after ablation based on data from the Biotronik ICM (BioMonitor3® or future generation of Biotronik ICM).

Primary Outcome

In the present study AF burden will be assessed at 3-month intervals during the 12 months following the blanking period (3-months post-ablation), and the difference at the end of the follow-up period of one year will serve as the primary comparison outcome between the two treatment groups.

Interventions

  • DEVICE Insertable Cardiac Monitor

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2020-06-25
Est. Completion 2024-02-15
Phase NA
University of Rochester

636 total trials

What the finished NCT04190186 record still lists

NCT04190186 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Insertable Cardiac Monitor is the first listed.

NCT04190186 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04190186 about?

NCT04190186 is a clinical study titled "Hybrid Ablation Plus Medical Therapy for Persistent Atrial Fibrillation". This clinical trial is designed to compare two management strategies for the treatment of asymptomatic/subclinical atrial fibrillation after ablation based on data from the Biotronik ICM (BioMonitor3® or future generation of Biotronik ICM).

What is the current status of trial NCT04190186?

This trial is currently completed. It is a NA study. The enrollment target is 55 participants. The study started on 2020-06-25. Estimated completion is 2024-02-15.

What interventions are being tested in trial NCT04190186?

The interventions under investigation include: Insertable Cardiac Monitor (DEVICE).

Who is sponsoring clinical trial NCT04190186?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04190186's enrollment target sits among peer trials

55 1264th of 2000 higher than 733 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 NCT04190186, the US trial registry maintained by the National Library of Medicine. NCT04190186 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.