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Artificial Intelligence Based Rapid Identification of ST-elevation Myocardial Infarction Using Electrocardiogram (ARISE)

Artificial Intelligence Based Rapid Identification of ST-elevation Myocardial Infarction Using Electrocardiogram (ARISE)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05118009
Enrollment
43176
Registered
2021-11-11
Start date
2022-05-01
Completion date
2023-05-31
Last updated
2023-06-22

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

Conditions

Myocardial Infarction, Acute

Brief summary

This is a randomized controlled trial (RCT) to test a novel artificial intelligence (AI)-enabled electrocardiogram (ECG)-based supporting tool for improving the diagnosis and management of ST-elevation myocardial infarction.

Interventions

Primary care clinicians in the intervention group had access to the report, which displayed whether the AI-ECG result was positive or negative.The system will send a message to corresponding physicians if positive finding.

Sponsors

National Defense Medical Center, Taiwan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients in emergency department or inpatient department. * Patients recieved at least 1 ECG examination.

Exclusion criteria

* The patients recieved ECG at the period of inactive AI-ECG system.

Design outcomes

Primary

MeasureTime frameDescription
E2C (ECG to coronary angiography) timeWithin 6 hoursTime from ECG to activation of coronary angiography for STEMI patients.

Secondary

MeasureTime frameDescription
D2B (Door to Balloon Time) timeWithin 6 hoursTime from first medical contact to complete of primary percutaneous coronary intervention for STEMI patients in emergency department.
D2C (Door to coronary angiography) timeWithin 6 hoursTime from first medical contact to activation of coronary angiography for STEMI patients in emergency department.
Ejection fractrionWithin 3 daysEjection fractrion primary percutaneous coronary intervention for STEMI patients.
E2B (ECG to primary percutaneous coronary intervention) timeWithin 6 hoursTime from ECG to complete of primary percutaneous coronary intervention for STEMI patients.
Highest concentration of creatine kinaseWithin 3 daysAfter performing an electrocardiogram, the highest concentration of creatine kinase was followed.
Length of hospitalizationWithin 28 daysAfter performing an electrocardiogram, the length of hospitalization.
Number of CAG eventWithin 6 hoursNumber of CAG event
Highest concentration of high-sensitivity cardiac troponin IWithin 3 daysAfter performing an electrocardiogram, the highest concentration of high-sensitivity cardiac troponin I was followed.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026