Clin2
NCT05459233Possibly a fitRecruiting

Testing ultrasound-guided valve settings after valve-in-valve TAVR

Aortic Valve StenosisAortic Valve RegurgitationProsthesis Failure

Part of Heart & circulation clinical trials.

This trial compares two ways to check and fine-tune how well a new valve is working after a “valve-in-valve” TAVR procedure. It looks to see whether measurements from ultrasound of the heart (Doppler echocardiography) match results from a catheter test, which could help guide safer, more accurate valve care.

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

Phase
N/A
Enrollment
310 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have a failing surgical aortic bioprosthetic (non-mechanical) valve that the care team approved for a valve-in-valve TAVR
  • Your prior surgical valve must be a stented (not stentless) type and its labeled size must be 25 mm or smaller
  • Your new valve-in-valve TAVR must use the SAPIEN 3 Ultra valve
  • You must not have certain valve types (stentless/sutureless, Trifecta, or Hancock II)
  • You must not be at high risk for blockage of the coronary arteries (as judged by CT distance to the coronary arteries or the Heart Team)
  • You must be able to sign written consent to join the study

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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