Status:
UNKNOWN
A Study of Low Dose vs Standard Ticagrelor on Platelet Function After Intervention for Acute Coronary Syndrome in Senior Patients
Lead Sponsor:
Shanghai Tong Ren Hospital
Conditions:
Senior Acute Coronary Syndrome Patients After PCI
Eligibility:
All Genders
75+ years
Phase:
PHASE4
Brief Summary
In this study, the investigates try to confirm our hypothesis that low dose ticagrelor(60mg) had similar anti-platelets function compared with the standard dose ticagrelor in senior （no less than 75 y...
Eligibility Criteria
Inclusion
- Subject must be at least 75 years of age 2 Patients should have undergone successful percutaneous coronary intervention with drug-eluting stent for acute coronary syndrome 3.Subject understand the study requirements and the treatment procedures and provided informed consent before the procedure
Exclusion
- Female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study
- Active bleeding
- Known hypersensitivity or contraindication to study medications
- Female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study
- Non-cardiac co-morbid conditions are present with life expectancy \<2 year or that may result in protocol non-compliance (per site investigator's medical judgment).
- Subjects with Cerebral hemorrhage history
- Subjects with stroke history in half a year
- subjects with active malignant tumor
- subjects with whom oral anticoagulants are needed
- Other conditions which the investigators think not applicable to the study.
Key Trial Info
Start Date :
March 10 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2024
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT04307485
Start Date
March 10 2020
End Date
July 1 2024
Last Update
October 6 2023
Active Locations (1)
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1
shanghai Tongren hospital
Shanghai, Shanghai Municipality, China, 200336