Clin2
NCT05681702Possibly a fitRecruiting

Personalizing medicines to reduce bleeding after stent procedure

Coronary Artery Disease

Part of Heart & circulation clinical trials.

This trial studies ways to reduce bleeding in people after a stent procedure (PCI) who have been taking two anti-platelet medicines (aspirin plus prasugrel or ticagrelor) for a set amount of time. It may help find a safer plan for preventing blood clots while lowering bleeding risk.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
90 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older
  • You had a stent procedure (PCI) and have been on aspirin 81 mg plus prasugrel or ticagrelor as maintenance treatment
  • You have been on this double medicine at least 30 days (if ongoing stable symptoms) or 3 months or longer (if you had an acute event)
  • You can sign a written informed consent form
  • You have not had a stent clot before, and you are not taking blood thinners like warfarin, apixaban, rivaroxaban, dabigatran, edoxaban, or long-term injections for clot treatment
  • You do not have major bleeding/bleeding-clotting problems, severe liver or kidney problems on dialysis, uncontrolled body instability, known medicine allergy to clopidogrel, or pregnancy/breastfeeding

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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