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RECRUITING
NCT05638867
PHASE4

NOAC Therapy Guided by PARIS Risk Score and D-dimer in Patients With ACS After PCI

Sponsor: China National Center for Cardiovascular Diseases

View on ClinicalTrials.gov

Summary

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.

Official title: A Randomized Controlled Clinical Trial of PARIS Coronary Thrombosis Risk Score Combined With D-dimer to Guide New Oral Anticoagulant Antithrombotic Therapy in Patients With Acute Coronary Syndrome After Percutaneous Coronary Intervention

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

3944

Start Date

2023-11-25

Completion Date

2027-01

Last Updated

2024-01-17

Healthy Volunteers

No

Interventions

DRUG

Aspirin + Clopidogrel + Rivaroxaban

Triple antithrombotic therapy: aspirin 75-100 mg orally once daily, clopidogrel 75 mg orally once daily, and rivaroxaban 2.5 mg orally twice daily

DRUG

Aspirin + Clopidogrel

Dual antithrombotic therapy: aspirin 75-100 mg orally once daily, clopidogrel 75 mg orally once daily

Locations (1)

Chinese Academy of Medical Sciences, Fuwai Hospital

Beijing, Beijing Municipality, China