Clinical Trials in China / NCT06686940
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Observational
Photoplethysmography (PPG) Algorithm With Smartwatch in Evaluation of Atrial Fibrillation Burden
NCT06686940 · tracked via the Priya Life Science China tracker
Condition(s) studied
Atrial Fibrillation (AF)
Investigational drug(s) / intervention(s)
intervention group
intervention group: The monitoring effect of a smart electrocardiogram watch based on the PPG algorithm on atrial fibrillation burden.
Study summary
The purpose of this study is to evaluate the monitoring effect of a smart electrocardiogram watch based on the PPG algorithm on atrial fibrillation burden.
Eligibility
Inclusion Criteria:
1. Atrial fibrillation patients diagnosed by electrocardiogram
2. Willing to use long-range electrocardiogram monitoring equipment
Exclusion Criteria:
1.Patients who are allergic to electronic devices or unable to wear watches
Primary outcome measure(s)
- Primary outcome — December 30, 2024 to Decemberr 30, 2034
all-cause death, cardiovascular death, myocardial infarction, heart failure, stroke, peripheral vascular disease, recurrence of atrial fibrillation diagnosed by electrocardiogram, palpitations symptoms
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Anzhen Hospital | Beijing | Beijing Municipality |
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Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06686940 on ClinicalTrials.gov ↗ ← All trials in China