REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve failuRE

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-105
SponsorMedtronic Cardiovascular

About this trial

The purpose of this study is to generate clinical evidence on valve safety and performance in subjects treated by redo Transcatheter Aortic Valve Replacement (TAVR).

Eligibility criteria

Qualifiers

BVF of a TAV (either Medtronic or Edwards) requiring redo TAVR

Disqualifiers

BVF due solely to paravalvular regurgitation

Active endocarditis

Untreated acute valve thrombosis

Life-expectancy less than 1-year

Trial design

Treatments tested in this trial

  • Medtronic TAV
  • Edwards TAV

Treatment groups

225 Participants
are divided into 1 treatment group

Sponsors and collaborators