Condition: Coronary Artery Disease · Percutaneous Coronary Intervention · Acute Coronary Syndrome · Sponsor: China National Center for Cardiovascular Diseases
The goal of this clinical trial is to compare short-term Triple Antithrombotic Therapy (DAPT + Rivaroxaban) followed by DAPT with standard DAPT in selected ACS patients with high ischemic risk. The main questions it aims to answer are: * Whether the intervention is effective in reducing ischemic events * Whether the intervention is safe from increasing bleeding events, especially severe or fatal ones Participants will be randomized to receive standard DAPT therapy for the entire study duration or low-dose rivaroxaban+DAPT for 3 months, followed by standard DAPT for the rest of the study duration. Patients enrolled should complete 5 follow-ups in the form of clinic visit or telephone call.
This description comes directly from the study's public registry record.
Jinqing Yuan, MD · +86-10-68314466 · dr_jinqingyuan@sina.com
Always discuss trial participation with your own doctor first.
| Chinese Academy of Medical Sciences, Fuwai Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05638867