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NCT04414865

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

Recruiting now Last updated 4 June 2020
What this trial tests

trial testing VitaFlow™ Transcatheter Aortic Valve System in Aortic Valve Stenosis in 100 participants. Currently enrolling.

Timeline
26 April 2020
Primary endpoint
1 December 2021
30 December 2027

Quick facts

Lead sponsorShanghai MicroPort CardioFlow Medtech Co., Ltd.
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment100
Start date26 April 2020
Primary completion1 December 2021
Estimated completion30 December 2027
Sites2 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai MicroPort CardioFlow Medtech Co., Ltd.

Who can join

70 and older, any sex, with Aortic Valve Stenosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study objective is to evaluate safety and effectiveness/performance of the Microport™ CardioFlow VitaFlow™ Transcatheter Aortic Valve System for the treatment of severe aortic stenosis in the real world settings.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of VitaFlow™ Transcatheter Aortic Valve System

Trials testing the same drug.

Other recruiting trials for Aortic Valve Stenosis

Currently open trials in the same condition.

Other Shanghai MicroPort CardioFlow Medtech Co., Ltd. trials

Trials by the same sponsor.

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Data sources for this page

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