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Study identifier: NCT05936606 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Tailored Anti-platelet Therapy After DES Implantation in High-risk Patients

Condition: Coronary Artery Disease  ·  Sponsor: Yonsei University

PhaseNA
Planned participants3434
Who can joinAll sexes, 19 Years to 80 Years
Healthy volunteersNo

About this study

Clopidogrel monotherapy has been found effective in reducing ischaemic cardiovascular and haemorrhagic complications in patients with drug-eluting stent (DES) placement. However, concerns remain about the safety of long-term clopidogrel monotherapy in high-risk patients with HPR (high platelet reactivity) who do not respond adequately to clopidogrel. This study aims to evaluate the effectiveness of a patient-tailored antiplatelet therapy strategy that considers platelet aggregation in high-risk patients with DES placement beyond 12 months after stenting.

This description comes directly from the study's public registry record.

Talk to the study team

Byeong-Keuk Kim  ·  02-2228-8465  ·  kimbk@yuhs.ac

Always discuss trial participation with your own doctor first.

Locations (1)

Severance HospitalSeoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT05936606