Clin2
NCT05677568Possibly a fitEnrolling by invitation

Registry study for Carillon device in leaky mitral valve

Functional Mitral RegurgitationMitral Regurgitation

Part of Heart & circulation clinical trials.

This registry collects health information from adults who already have the Carillon device to treat a leaky mitral valve caused by dilated heart muscle. The goal is to better understand how the device performs in real-world care over time.

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

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

Who can take part

  • You are at least 18 years old
  • You have functional mitral regurgitation (a leaky mitral valve due to enlarged/dilated heart muscle)
  • You already have the Carillon device implanted
  • You can sign and understand informed consent to join the registry
  • You have baseline heart test results from the registry plan, including: MR grade, LVEF %, LVEDD, LAD, and valve/heart measurements (AP and ML diameters), plus NYHA class

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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