Coronary Artery Disease Clinical Trial
Official title:
A Large, Prospective, Randomized, Multicenter Clinical Study Evaluating the Safety and Efficacy of the Post-marketing Drug-eluting Stent System (Rapamycin) - the EXCROSSAL Stent in CAD Patients With 3-month DAPT or 12-month DAPT
1. Prospective, randomized, multicenter clinical study
2. This is a post-marketing clinical study to evaluate whether it will affect the safety
event when it is used in different treatment ways. Adopting non - inferiority design,
2700 cases were enrolled.
3. EDC system (eCRF electronic data collection system)
4. Follow-up points: 30 days,3 months, 12 months, 24 months, 36 months, 48 months and 60
months after the operation;
1. Subjects are eligible for coronary intervention
2. The lesion needs to be pre-expanded or special circumstances should be carefully
considered according to the clinical manifestations
3. The selection of target vessel is based on the criteria of a diameter between 2.25mm and
4.0mm
4. If a stent needs to be placed at the target vessel, it is recommended that there be at
least 2mm overlap between the stents; if the stent expansion is not sufficient,
post-dilatation treatment is required.
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