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Arrhythmias Syncope is Diagnosed by Wearable Intelligent ECG Monitoring Device

Arrhythmias Syncope is Diagnosed by Wearable Intelligent ECG Monitoring Device

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-DDD-16009981
Enrollment
Unknown
Registered
2016-11-23
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

arrhythmias syncope

Interventions

Gold Standard:
Index test:

Sponsors

Shanghai First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. the patients who have syncope twice per week; 2. aged 18 to 60 years.

Exclusion criteria

Exclusion criteria: 1. ischemic stroke; 2. heart valve disease; 3. left atrial myxoma; 4. hypertrophic obstructive cardiomyopathy; 5. Left ventricular ejection fraction <40%; 6. Moderate and severe anemia; 7. Severe pulmonary disease; 8. Severe liver and kidney dysfunction; 9. Severe mental illness; 10. Poor quality of ECG; 11. the patients who are unable to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Diagnostic rate of arrhythmia syncope;

Countries

China

Contacts

Public ContactLiqun Zhao

Department of Cardiology, Shanghai First People's Hospital

zhaoliq8570@hotmail.com+86 13482528734

Outcome results

None listed

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