A Fib Clinic of the Future Using KardiaPro Platform for Chronic Care of Patients With AF After Ablation Procedure
Completed · Not applicable
Conditions studied: Atrial Fibrillation
In brief
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.
Key facts
- Study ID
- NCT03557034
- Run by
- The Cleveland Clinic
- People needed
- 100
- Starts
- 2018-06-27
- Expected to finish
- 2020-08-15
- Last updated by the study team
- 2021-07-15
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18-85 years old
- Have smartphone with data plan
- History of AF (paroxysmal or persistent)
- In sinus rhythm at the 3-4 month post-procedure visit and no evidence of AF during the interval starting after the 3 week blanking period and ending at the appointment time.
- On Anticoagulation if CHADS VASC score is ≥ 1 and will continue to be on anticoagulation or CHADS VASC of Zero
- Willing to follow up with their Cleveland Clinic electrophysiologist in 6 months
You may not qualify if…
- Patients without smartphone
- Unwilling to provide consent
- Unwilling to follow up in 6 months
- CHADS VASC ≥ 1 and anticoagulation will be stopped
- Presence of a cardiac implantable electronic device
- If the primary electrophysiologist decides the patient still needs monitoring through traditional monitors due to any reason
Where it is running
- Cleveland Clinic — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
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