Efficacy and Safety of Low-dose Ticagrelor

NCT03381742 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 3043

Last updated 2019-09-30

Study results available
· View outcomes & findings →

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03381742 on ClinicalTrials.gov