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NCT03557034 · ClinicalTrials.gov registry record · NA

A Fib Clinic of the Future Using KardiaPro Platform for Chronic Care of Patients With AF After Ablation Procedure

A NA study, sponsored by The Cleveland Clinic.

Completed
Registry status
NA
Development phase
100
Enrollment target

NCT03557034: Completed NA study, sponsored by The Cleveland Clinic.

NCT03557034 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03557034, a NA study, has completed, sponsored by The Cleveland Clinic.

COMPLETED
Registry status
NA
Development phase
100 participants
Enrollment target

Study Summary

Pulmonary vein isolation is a widely used strategy for the treatment of patients with symptomatic atrial fibrillation. After successful pulmonary vein isolation (no atrial fibrillation on transtelephonic rhythm recordings for 3 months following ablation), heart rhythm is not routinely monitored. The goal of this study is to determine whether the Kardia Mobile device detects AF at a different rate compared to our standard of care. The study also hopes to understand how this Kardia Mobile device and Kardia Pro platform affect health care utilization and patient anxiety.

Primary Outcome

This outcome will measure the time between the ablation procedure (time zero) and the time of first detected atrial fibrillation heart rhythm.

Interventions

  • DEVICE Kardia Monitoring

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2018-06-27
Est. Completion 2020-08-15
Phase NA
The Cleveland Clinic

688 total trials

What the finished NCT03557034 record still lists

NCT03557034 is an interventional study that assigns participants to a tested intervention. The registered 100 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 (93% lower).

The record links to 0 conditions, and to 1 intervention - of which Kardia Monitoring is the first listed.

NCT03557034 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03557034 about?

NCT03557034 is a clinical study titled "A Fib Clinic of the Future Using KardiaPro Platform for Chronic Care of Patients With AF After Ablation Procedure". Pulmonary vein isolation is a widely used strategy for the treatment of patients with symptomatic atrial fibrillation. After successful pulmonary vein isolation (no atrial fibrillation on transtelephonic rhythm recordings for 3 months following ablation), heart rhythm is not routinely monitored. The...

What is the current status of trial NCT03557034?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2018-06-27. Estimated completion is 2020-08-15.

What interventions are being tested in trial NCT03557034?

The interventions under investigation include: Kardia Monitoring (DEVICE).

Who is sponsoring clinical trial NCT03557034?

This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03557034's enrollment target sits among peer trials

100 840th of 2000 higher than 1,081 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 NCT03557034, the US trial registry maintained by the National Library of Medicine. NCT03557034 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.