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Diagnostic Efficacy of Long-term Implantable Cardiac Monitors for Recurrent Atrial Fibrillation

Diagnostic Efficacy of Long-term Implantable Cardiac Monitors for Recurrent Atrial Fibrillation in Patients Undergoing Catheter Ablation for Atrial Fibrillation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009385
Enrollment
100
Registered
2024-05-02
Start date
2024-05-31
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : Participants in the study will be equipped with both a long-term wearable cardiac monitor (Mobicare) and a 24-hour Holter monitor simultaneously. After 7days, the devices will be retu

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Diagnosis of atrial fibrillation Undergoing radiofrequency ablation or cryoablation for atrial fibrillation

Exclusion criteria

Exclusion criteria: Hypersensitivity to the adhesive ECG monitor

Design outcomes

Primary

MeasureTime frame
Detection rate of atrial fibrillation (or atrial tachycardia)

Secondary

MeasureTime frame
Detection rate of supraventricular tachycardia, bradyarrhythmia, or ventricular tachycardia

Countries

Korea, Republic of

Contacts

Public ContactYoung Choi

The Catholic University of Korea, Seoul St. Mary's Hospital

coolnite0@gmail.com+82-2-1588-1511

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026