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VitaFlow Transcatheter Aortic Valve System Post-market Study-The LAUNCH Study

VitaFlow Transcatheter Aortic Valve System Post-market Study-The LAUNCH Study

Recruiting
70 years and older
All
Phase N/A
  • Simplified description (AI rewritten)
  • Technical description (Original)

This is a prospective, single-arm, multi-center, observational, post-market registry study. The purpose is to evaluate the safety, performance, and effectiveness of the VitaFlow Transcatheter Aortic Valve System in the real world settings.Patients will be seen at pre and post procedure, discharge, 30 days, 1 year and annually up to 5 years.

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Study details
    Aortic Stenosis
    VALVULAR HEART DISEASE

NCT04414865

Shanghai MicroPort CardioFlow Medtech Co., Ltd.

19 February 2024

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