Clin2
NCT07840365Likely a fitRecruiting

Finding the best blood-thinner plan after a Watchman device procedure

Atrial Fibrillation (AF)

Part of Heart & circulation clinical trials.

This study tests which blood-thinner approach works best after a procedure to close a small heart pouch (left atrial appendage) with a Watchman device. It aims to prevent strokes while reducing bleeding risks.

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

Phase
Phase 3
Enrollment
234 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older.
  • You have had a successful procedure to close a heart pouch (left atrial appendage) with a Watchman device, or you are scheduled to have it.
  • You have atrial fibrillation (irregular heartbeat) - whether it comes and goes, persists, or is permanent.
  • You do not have other conditions that require you to take blood thinners for reasons other than atrial fibrillation.
  • You are not allergic to aspirin, clopidogrel, or apixaban, and you have not had recent major bleeding or surgery, a recent heart attack, or a recent blood clot.

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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