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VitaFlow II Transcatheter Aortic Valve System Pre-market Trial

VitaFlow II Transcatheter Aortic Valve System Pre-market Trial

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

This a prospective, multi-center, single-arm, objective performance clinical investigation, aiming to evaluate the safety and effectiveness of Microport CardioFlow VitaFlow II Transcatheter Aortic Valve System for the treatment of severe aortic stenosis. A total of 145 subjects will be enrolled in 18 clinical centers within China. Clinical or telephone follow-up is scheduled at 30 days, 6 months, 12 months, and 2-5 years after valve implantation.

Study details
    Aortic Stenosis
    VALVULAR HEART DISEASE

NCT04414878

Shanghai MicroPort CardioFlow Medtech Co., Ltd.

19 February 2024

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