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NCT06465706Likely a fitNot yet recruiting

Testing safety and effectiveness of LAmbre Plus device for AFib

Atrial Fibrillation

Part of Heart & circulation clinical trials.

This trial tests a new device (LAmbre Plus) that closes off a small pouch in the heart (left atrial appendage) to reduce stroke risk in people with AFib who cannot take blood thinners long-term. The procedure is an alternative to daily medication.

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

Phase
N/A
Enrollment
1,826 people
Ages
18 years to 100 years
Study type
Interventional

Who can take part

  • You must be 18 years or older and not pregnant or nursing.
  • You must have a type of atrial fibrillation (AFib) that is not caused by a short-term issue like surgery or infection.
  • You must have a moderate to high risk of stroke, as measured by a CHADS2 or CHA2DS2-VASc score.
  • Your doctor must agree that a short course of blood thinner (warfarin) is safe for you, but a non-medication approach is better long-term.
  • Your heart team (including a cardiologist) must decide together that this procedure is right for you.
  • You must not have certain heart valve problems, recent stroke or heart attack, or other major health issues that would make the procedure unsafe.

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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