Low-dose Ticagrelor in Chinese ACS Patients Undergoing PCI
Launched by FIRST AFFILIATED HOSPITAL OF HARBIN MEDICAL UNIVERSITY · Dec 20, 2017
Trial Information
Current as of April 24, 2025
Unknown status
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • After half-dose ticagrelor (loading dose 90mg, and then 45mg bidpo.) treatment for 3 days, the platelet aggregation is effectively inhibited by light transmission aggregometry method and thromboela-stogram.
- • planned to undergo PCI recently
- • planned to DAPT for 1 year after PCI
- Exclusion Criteria:
- • taken adenosine diphosphate (ADP) receptor antagonists within 2 weeks
- • Platelet count \<100g/L;
- • A history of bleeding tendency;
- • Aspirin, ticagrelor or clopidogrel allergies;
- • Severe liver injury.
Trial Officials
Yue Li, PhD
Principal Investigator
Cardiovascular Department, the First Affiliated Hospital of Harbin Medical University
About First Affiliated Hospital Of Harbin Medical University
The First Affiliated Hospital of Harbin Medical University is a leading clinical research institution dedicated to advancing healthcare through innovative medical studies and trials. As a prominent teaching hospital in China, it combines cutting-edge research with comprehensive patient care, facilitating a robust environment for clinical investigations across various medical disciplines. The hospital is committed to improving clinical outcomes and enhancing patient safety, fostering collaboration among healthcare professionals, researchers, and industry partners. With a focus on translating research findings into practice, the First Affiliated Hospital plays a vital role in the development of new treatments and therapies, contributing to the global body of medical knowledge.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, , China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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