Long-Term Follow-Up in Patients With Acute Myocardial Infarction Cohort
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Treatment Strategies.
- Who it may be relevant to
- Registry conditions: Acute Myocardial Infarction, Adverse Event. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Long-Term Follow-Up in Patients With Acute Myocardial Infarction Cohort - a Prospective, Multicenter Study
Overview
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.
Interventions
- Other Treatment Strategies
AMI emergency treatment process, pre-reperfusion medication, reperfusion strategy selection, and early cardiac rehabilitation after reperfusion
Primary outcome measures
- Incidence of MACCE [Time frame: 5 years after discharge]
Secondary outcome measures (4)
- Differences of MACCE between the optimized group and the non-optimized group [Time frame: 5 years after discharge]
- Differences of the MACCE between OCT-guided group and the coronary angiography -guided group [Time frame: 5 years after discharge]
- Differences of MACCE between defer PCI group and direct PCI group [Time frame: 3 and 5 years after discharge]
- Differences of the MACCE incidence between cardiac rehabilitation quality improvement group and non-cardiac rehabilitation group [Time frame: 5 years after discharge]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
China · 18 centers
- Beijing An Zhen Hospital, Capital Medical University — Beijing
- Beijing Chao-Yang Hospital, Capital Medical University — Beijing
- Peking University First Hospital — Beijing
- Guangdong general hospital — Guangzhou
- The first affiliated hospital of Guangxi medical university — Nanning
- Second hospital of hebei medical university — Shijiazhuang
- Daqing Oil Field Hospital — Daqing
- The First Affiliated Hospital of Zhengzhou University — Zhengzhou
- … and 10 more centers
Identifiers
NCT: NCT05862103 · KY2022-266