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AWARE Registry: Wearable ECG in Structural Heart Interventions

Not yet recruiting
Conditions
Patent Foramen Ovale
Atrial Septal Defect
Registration Number
NCT06236776
Lead Sponsor
Yonsei University
Brief Summary

This study is a multi-center (Sinchon Severance hospital / Gangnam Severance hospital), prospective cohort observational study to patients who had undergone structural heart intervention including device closure for secundum type atrial septal defect or Patent foramen ovale. Transthoracic echocardiography will be performed before the procedure, immediately after, and at 6, 18, 30 months after the procedure. Wearable ECG monitoring (\> 3 days) will be performed before the procedure or immediately after procedure. Demographic, laboratory, hemodynamic data during procedure, and non-invasive imaging dat are obtained.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Adult ≥ 19 year-old
  • Patients who scheduled to perform percutaneous device closure for atrial septal defect or patent foramen ovale
  • Patients provided with the written, informed consent to participate in this study
Exclusion Criteria
  • Patients who had paroxysmal, persistent, or chronic AF
  • Life expectancy < 12 months
  • Subject who the investigator deems inappropriate to participate in this study

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Occurrence of atrial fibrillation30 month

Occurrence of atrial fibrillation at Immediate post-operative, 18, and 30 month on wearable ECG monitoring

Secondary Outcome Measures
NameTimeMethod
All cause-deathImmediate post-operative, 18 month , 30 month
hospitalization for heart failureImmediate post-operative, 18 month , 30 month

hospitalization for heart failure: data from electronic medical record in Yonsei university health system

new atrial tachycardiaImmediate post-operative, 18 month , 30 month
high burden of APC/PVC (>15%)Immediate post-operative, 18 month , 30 month

high burden of APC/PVC ( \>15%): on wearable ECG monitoring

new atrial fibrillationImmediate post-operative, 18 month , 30 month

Trial Locations

Locations (1)

Division of Cardiology, Yonsei University Health System, Yonsei University College of Medicine

🇰🇷

Seoul, Korea, Republic of

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