Clin2
NCT07575867Possibly a fitRecruiting

Reduced Blood Thinner Strategy After Heart Device Closure

Atrial FibrillationStroke Prevention in Patients With Atrial FibrillationLeft Atrial Appendage ClosureHemorrhageAnticoagulants / Administration & DosageReduced-dose ApixabanThromboembolism

Treatments studied

Part of Heart & circulation clinical trials.

This trial tests whether patients who receive a special device to close a hole in the heart (to prevent stroke from irregular heartbeat) can safely take fewer blood-thinning medications afterward. The study compares taking a standard blood thinner for 3 months versus taking aspirin only, to see which approach works best with fewer bleeding risks.

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

Phase
N/A
Enrollment
464 people
Ages
18 years and older
Study type
Observational

Who can take part

  • Age 18 or older
  • Diagnosed with atrial fibrillation (irregular heartbeat) documented on heart rhythm test in the past 12 months
  • Medium-to-high stroke risk based on health factors (score ≥3 for women, ≥2 for men)
  • Able to tolerate apixaban (a blood thinner) for at least 3 months
  • No recent heart attack, stroke, or major bleeding within 30 days before the procedure
  • Successful completion of the heart device closure procedure with no major leaks

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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