Skip to content

Efficacy and safety of reduced dose ticagrelor in patients treated with drug-eluting stents

Efficacy and safety of reduced dose ticagrelor in patients treated with drug-eluting stents: A results from the Work Of New anti-thrombotic therapy in patients treated with Ticagrelor (WON-T) observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011909
Enrollment
244
Registered
2026-04-27
Start date
2024-12-01
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Wonkwang University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed with acute coronary syndrome who have undergone successful percutaneous coronary intervention with drug-eluting stent implantation 2) Patients who voluntarily agree to participate in the study and provide written informed consent

Exclusion criteria

Exclusion criteria: 1) Age < 19 years 2) Patients who received loading treatment with clopidogrel or prasugrel prior to the index procedure 3) Contraindications to ticagrelor, including a history of intracranial hemorrhage or active bleeding 4) Patients with an expected life expectancy of less than 1 year 5) Patients deemed inappropriate for study participation at the discretion of the investigator

Design outcomes

Primary

MeasureTime frame
Target vessel failure (cardiac death, target vessel myocardial infarction, target vessel revascularization)

Secondary

MeasureTime frame
Major adverse cardiovascular event (all cause death, myocardial infarction, stroke, any revascularization)

Countries

Korea, Republic of

Contacts

Public ContactKyeong Ho Yun

Wonkwang University Hospital

dryunkh@gmail.com+82-63-859-2524

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: May 7, 2026