Efficacy and Safety of Low-dose Ticagrelor
NCT03381742 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 3043
Last updated 2019-09-30
Summary
Guideline recommendations on the use of dual antiplatelet therapy have been formulated that ticagrelor 90 mg twice daily plus aspirin in preference to clopidogrel 75mg daily plus aspirin for ACS patients. Recent study found that ticagrelor 90mg twice a day orally could significantly reduce the occurrence of clopidogrel resistance and adverse cardiovascular events. The previous studies have reported that half-dose ticagrelor had the similar inhibitory effect on platelet aggregation as the standard-dose ticagrelor, which was significantly stronger than that in the clopidogrel group. One-quarter standard-dose ticagrelor provided greater degree of platelet inhibition than standard dose clopidogrel in Chinese patients with stable CAD. But large-scale clinical trials are still needed to confirm the effects of low-dose ticagrelor on platelet function in Chinese patients with coronary heart disease.
Conditions
Interventions
- DRUG
-
Ticagrelor
ticagrelor 45 mg twice daily for 5 consecutive days at least.
- DRUG
-
ticagrelor
ticagrelor 90 mg once daily for 5 consecutive days at least.
- DRUG
-
ticagrelor
ticagrelor 90 mg twice daily for 5 consecutive days at least.
- DRUG
-
clopidogrel
clopidogrel 75 mg once daily for 5 consecutive days at least.
Sponsors & Collaborators
-
Beijing Anzhen Hospital
collaborator OTHER -
The First Affiliated Hospital of Dalian Medical University
collaborator OTHER -
The Central Hospital of Jia Mu Si City
collaborator UNKNOWN -
First Affiliated Hospital of Kunming Medical University
collaborator OTHER -
RenJi Hospital
collaborator OTHER -
Tianjin Medical University General Hospital
collaborator OTHER -
Weifang People's Hospital
collaborator OTHER -
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
collaborator OTHER -
Shengjing Hospital
collaborator OTHER -
Shaanxi Provincial People's Hospital
collaborator OTHER -
First Affiliated Hospital of Harbin Medical University
lead OTHER
Principal Investigators
-
Yue Li, MD · Cardiovascular Department, the First Affiliated Hospital of Harbin Medical University
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-12-13
- Primary Completion
- 2018-12-13
- Completion
- 2019-02-13
Countries
- China
Study Locations
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