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P2Y12 receptor inhibitor

ticagrelor for Coronary Artery Disease

Phase 2 & 3
Waitlist Available
Research Sponsored by First Affiliated Hospital of Harbin Medical University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 7 days, 1 month, 3 months, 6 months and 12 months
Awards & highlights

Study Summary

With the widespread use of clopidogrel, resistance to clopidogrel has been attracting increasing attention, and emerged as a new challenge adversely affecting patients clinical risk and outcome. Clopidogrel resistance means that blood platelets show little or no response to clopidogrel. It is closely associated with increased risk of serious cardiovascular events, seriously affects the prognosis of patients, and brings difficulties to clinical treatment. 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. But it is still not very clear that the effect of low-dose ticagrelor on platelet function in patients with clopidogrel resistance and coronary heart disease. Therefore, we performed this randomized, single-blind clinical trial to observe the effects of low-dose ticagrelor and double standard-dose clopidogrel on platelet aggregation and prognosis in clopidogrel resistance's patients with coronary heart disease.

Eligible Conditions
  • Coronary Artery Disease
  • Clopidogrel Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 7 days, 1 month, 3 months, 6 months and 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 7 days, 1 month, 3 months, 6 months and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
The platelet aggregation rate
Secondary outcome measures
Adverse events including myocardial infarction, death, stroke, re-hospitalization for cardiovascular diseases and ischemia events
Side effects including bleeding,dyspnea and arrhythmia

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: ticagrelorExperimental Treatment1 Intervention
To observe low-dose of ticagrelor on platelet aggregation in clopidogrel resistance's patients with coronary heart disease
Group II: clopidogrelActive Control1 Intervention
To observe double standard-dose clopidogrel on platelet aggregation in clopidogrel resistance's patients with coronary heart disease
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ticagrelor
FDA approved

Find a Location

Who is running the clinical trial?

First Affiliated Hospital of Harbin Medical UniversityLead Sponsor
136 Previous Clinical Trials
1,370,307 Total Patients Enrolled
9 Trials studying Coronary Artery Disease
7,276 Patients Enrolled for Coronary Artery Disease

Frequently Asked Questions

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~10 spots leftby Apr 2025