Condition: Acute Myocardial Infarction · Adverse Event · Sponsor: Yu Bo
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.
This description comes directly from the study's public registry record.
Xiling Zhang, MD · +86 13804608748 · xlzhangdr@163.com
Always discuss trial participation with your own doctor first.
| Beijing An Zhen Hospital, Capital Medical University | Beijing, Beijing Municipality, China | Recruiting |
| Beijing Chao-Yang Hospital, Capital Medical University | Beijing, Beijing Municipality, China | Recruiting |
| Peking University First Hospital | Beijing, Beijing Municipality, China | Not Yet Recruiting |
| Guangdong general hospital | Guangzhou, Guangdong, China | Recruiting |
| The first affiliated hospital of Guangxi medical university | Nanning, Guangxi, China | Recruiting |
| Second hospital of hebei medical university | Shijiazhuang, Hebei, China | Recruiting |
| Daqing Oil Field Hospital | Daqing, Heilongjiang, China | Recruiting |
| The First Affiliated Hospital of Zhengzhou University | Zhengzhou, Henan, China | Recruiting |
| Zhongda Hospital Southeast University | Nanjing, Jiangsu, China | Recruiting |
| The Second Affiliated Hospital of Nanchang University | Nanchang, Jiangxi, China | Recruiting |
| The Second Hospital of Jilin University | Changchun, Jilin, China | Recruiting |
| The econd Affiliated Hospital of Dalian Medical University | Dalian, Liaoning, China | Recruiting |
+ 6 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05862103