Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
TERMINATED
NCT03729401
PHASE4

Personalization of Long-Term Antiplatelet Therapy - RAPID EXTEND

Sponsor: Ottawa Heart Institute Research Corporation

View on ClinicalTrials.gov

Summary

In patients after myocardial infarction (MI) (heart attacks) and treated with percutaneous coronary intervention (PCI), the current standard is dual antiplatelet therapy (DAPT), with aspirin and a P2Y12 receptor inhibitor, for 1 year of treatment. At 1 year, there are several options including: i) Ongoing DAPT (with aspirin and ticagrelor), ii) Selective treatment use of a P2Y12 inhibitor based on risk profiles. This study is a pilot vanguard study to evaluate several strategies for choosing anti-platelet regimen among patients post MI and PCI at 1 year.

Official title: Personalization of Long-Term Antiplatelet Therapy Using a Novel Combined Demographic/Pharmacogenomic Strategy - The RAPID EXTEND Randomized Study

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

INTERVENTIONAL

Enrollment

39

Start Date

2019-08-22

Completion Date

2026-02-26

Last Updated

2026-05-06

Healthy Volunteers

No

Interventions

DRUG

Active Comparator: Dual Antiplatelet Therapy (DAPT) - Aspirin 81 mg + Ticagrelor 60mg twice daily

DAPT with aspirin and ticagrelor

DRUG

Ticagrelor Monotherapy: Ticagrelor 60 mg twice daily

Ticagrelor monotherapy

DRUG

Personalized Therapy Arm: Aspirin 81 mg or Ticagrelor 60mg twice daily or Clopidogrel 75 mg once daily

Personalized therapy based on risk score and genotyping

Locations (1)

University of Ottawa Heart Institute

Ottawa, Ontario, Canada