Long-Term Follow-Up in Patients With Acute Myocardial Infarction Cohort

Yu Bo

Status: Enrolling

Conditions: Adverse Event; Acute Myocardial Infarction

Treatments: Other: Treatment Strategies

Study type: Observational

Funder types: Other

Identifiers

NCT05862103

KY2022-266

Details and patient eligibility

About

AMI Survivors who participated in the project "Construction and key technology research of the whole myocardial protection system for acute myocardial infarction" (project number 2016YFC1301100) and completed the 1-year visit were followed up by telephone at 3 years (within the corresponding follow-up time window) and 5 years after discharge to acquire the patients' medication, health status, and major adverse cardiovascular and cerebrovascular events, including death, heart failure, rehospitalization, re-myocardial infarction, revascularization, stroke, malignant arrhythmia, and bleeding events.

Enrollment: 15,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• AMI survivors who participated in the project "Construction and key technology research of the whole myocardial protection system for acute myocardial infarction" and completed the 1-year visit.
• Telephone to obtain informed consent from the subjects/family members of the subjects.

Exclusion criteria

• Not available

Trial design

15,000 participants in 2 patient groups

optimized group

Description:

the patients received at least one optimized treatment

Treatment:

Other: Treatment Strategies

un-optimized group

Description:

the patients didn't receive optimized treatment