Actively Recruiting
Efficacy and Safety Study of Vicagrel in Patients With Acute Coronary Syndrome (ACS) Undergoing Percutaneous Coronary Intervention (PCI)
Led by Jiangsu vcare pharmaceutical technology co., LTD · Updated on 2024-10-01
1000
Participants Needed
1
Research Sites
120 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a multi-center, randomized, double-blind, double-dummy, parallel-controled, phase III trial, aiming to evaluate the effectiveness and safety of long-term continuous administration of Vicagrel capsules in ACS patients undergoing PCI.
CONDITIONS
Official Title
Efficacy and Safety Study of Vicagrel in Patients With Acute Coronary Syndrome (ACS) Undergoing Percutaneous Coronary Intervention (PCI)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between 18 and 80 years old, with no gender restrictions.
- Diagnosed with acute coronary syndrome (ACS) and scheduled for percutaneous coronary intervention (PCI), including STEMI and NSTE-ACS (UA/NSTEMI).
- Voluntarily sign the informed consent form and agree to follow all visit arrangements specified in the study protocol during the trial period.
You will not qualify if you...
- Expected survival time less than 12 months.
- Severe liver dysfunction not caused by heart disease, with ALT or AST levels more than 3 times the upper limit of normal, or cirrhosis.
- Pregnant or lactating women, or participants and their partners planning to become pregnant during the trial period.
- Other reasons as determined by researchers that make participation unsuitable.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
General Hospital of Northern Theater Command of Chinese PLA
Shenyang, Liaoning, China, 110015
Actively Recruiting
Research Team
X
Xiaojuan Lai
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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