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Observational study on detecting arrhythmia with OPPO intelligent wearable device (pre-test)

Observational study on detecting arrhythmia with OPPO intelligent wearable device (pre-test)

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056521
Enrollment
Unknown
Registered
2022-02-07
Start date
2022-02-07
Completion date
Unknown
Last updated
2024-10-07

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

Conditions

Cardiac Arrhythmias

Interventions

Observation group:None

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. The subject agrees to participate in the clinical study. 2. There were 50 subjects with normal sinus rhythm and no definite cardiovascular disease during screening, or the following arrhythmias existed during screening: sinus bradycardia in 50 subjects, frequent ventricular premature beats in 50 subjects, frequent atrial premature beats in 50 subjects, atrial fibrillation in 100 subjects, and sinus arrhythmia in 50 subjects. 3. Aged >= 18 years.

Exclusion criteria

Exclusion criteria: 1. Malignant arrhythmia (ventricular tachycardia, ventricular fibrillation, cardiac arrest); 2. In pregnancy or perinatal period; 3. There is abnormal pigment or skin disease around the measuring part that affects the wearing of the watch; 4. Unable to cooperate with the study due to mental illness, epilepsy or other reasons; 5. Implantation of permanent or temporary pacemakers.

Design outcomes

Primary

MeasureTime frame
ECG;

Countries

China

Contacts

Public ContactChen Erdong

Peking University First Hospital

lovemaster@vip.sina.com+86 13810836069

Outcome results

None listed

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