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Evaluation of Wearable Electrocardiogram Device Effectiveness in Myocardial Ischemia Detection (MiniECG-MID)

Evaluation of Wearable Electrocardiogram Device Effectiveness in Myocardial Ischemia Detection (MiniECG-MID)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112187
Enrollment
Unknown
Registered
2025-11-11
Start date
2025-11-20
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Myocardial Ischemia

Interventions

Chest pain patients with myocardial ischemia:N/A
Chest pain patients without myocardial ischemia:N/A

Sponsors

The University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients attend A&E of Queen Mary Hospital for chest pain.

Exclusion criteria

Exclusion criteria: 1. Unable to complete ECG belt examination due to illness or physical reasons. 2. Refuse to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Diagnostic accuracy of mini-ECG for ST-segment deviations;—

Secondary

MeasureTime frame
Diagnostic accuracy of mini-ECG for myocardial injury;Diagnostic accuracy of mini-ECG for severe coronary stenosis;Diagnostic accuracy of mini-ECG for occlusive myocardial infarction (OMI);—

Countries

China

Contacts

Public ContactTse Hung Fat

The University of Hong Kong

hftse@hku.hk+852 9837 5466

Outcome results

None listed

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