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Mobile ECG analysis prompt software clinical trial

Mobile ECG analysis prompt software clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095348
Enrollment
Unknown
Registered
2025-01-06
Start date
2022-05-05
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

atrial fibrilation

Interventions

Gold Standard:Digital 12-lead electrocardiograph
Index test:ECG Analyzer-1

Sponsors

University of Chinese Academy of Sciences Shenzhen Hospital (Guangming)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 93 Years

Inclusion criteria

Inclusion criteria: i.Age is older than 18 years old, gender is not limited; ii.People with arrhythmia or normal people; iii.Agree to participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: i.Those with skin allergies or ulcers on the wrist; ii.Patients with pacemakers; iii.Pregnant women; iv.Those with skin allergies to ethanol; v.Others who the researcher believes are not suitable to participate in the trial.

Design outcomes

Primary

MeasureTime frame
consistency rate;

Secondary

MeasureTime frame
Failure rate of test equipment;Single event consistency rate;

Countries

China

Contacts

Public ContactZhan Zhongqun

University of Chinese Academy of Sciences Shenzhen Hospital (Guangming)

zzqun21@126.com+86 199 2535 6161

Outcome results

None listed

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