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Effectiveness of Artificial Intelligent Based mHealth System to Reduce ACS Patients Bleeding Events After PCI

C

Chinese PLA General Hospital (301 Hospital)

Status

Unknown

Conditions

Percutaneous Coronary Intervention
Acute Coronary Syndrome
Bleeding

Treatments

Behavioral: AI based mHealth system

Study type

Interventional

Funder types

Other

Identifiers

NCT03738930
AI-mHealth-pilot

Details and patient eligibility

About

The present study was designed to observe the effectiveness of artificial intelligent based mHealth system(Chronic disease management system) to reduce bleeding events in ACS patients undergoing PCI.

Enrollment

420 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

age≥18 years, male or female; confirmed acute coronary syndrome patients; undergo percutaneous coronary intervention (PCI) treatment; good command of smart phones agree to participate in this clinical study and sign a written consent form.

Exclusion criteria

ACS admission deemed secondary to other cause such as traffic accidents, trauma, severe upper gastrointestinal bleeding, surgery, or procedure; patients who are not intend to attend 1 year of follow-up study or investigators find that patients are not able to comply with the study's requirements; pregnant women or lactating women; investigators consider patients who were not suitable for participation with other reasons

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

420 participants in 2 patient groups

normal follow-up group
No Intervention group
Description:
normal follow-up in ACS patients after PCI
AI based mHealth system follow-up group
Experimental group
Description:
AI based mHealth system follow-up in ACS patients after PCI. ACS patients in this group will receive message to take more notice to bleeding events.
Treatment:
Behavioral: AI based mHealth system

Trial contacts and locations

1

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Central trial contact

Yundai Chen, Master; Dandan Li, Master

Data sourced from clinicaltrials.gov

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