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REPAIR - transcatheteR rEPair of mitrAl Insufficiency With caRdioband System

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Contents

clinicaltrials.gov/study/NCT02703311
Is a
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Clinical study
0

Clinical Study attributes

NCT Number
NCT027033110
Health Conditions in Trial
‌
Mitral valve annuloplasty
0
Trial Recruitment Size
110
Trial Sponsor
Edwards Lifesciences
Edwards Lifesciences
0
Clinical Trial Start Date
2016
0
Primary Completion Date
2017
0
Study Completion Date
2018
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Device0
Intervention Name
Cardioband0
Interventional Trial Phase
Not Applicable0
Official Name
REPAIR - transcatheteR rEPair of mitrAl Insufficiency With caRdioband System0
Last Updated
November 9, 2020
0
Allocation Type
NA0
Intervention Model
Single Group Assignment0
Masking Type
None (Open Label)0
Study summary

The Cardioband Transcatheter System (Cardioband) is indicated for the treatment of secondary (functional) mitral regurgitation (FMR). The Cardioband is a transcatheter system, deployed on the beating heart through a transseptal approach. The Cardioband is deployed along the posterior annulus of the mitral valve (MV) and is adjusted under trans-esophageal guidance on the beating heart. A CE mark study with 30 subjects has been completed and documented reduction of severity of mitral regurgitation (MR) and improvement in 6- minute walk test in subjects with moderate to severe MR. Study objectives are to test the efficacy of the Cardioband in improving MR and heart failure symptoms in patients with symptomatic (New York Heart Association (NYHA) Class III-IVa), severe MR in the post-marketing setting, And to evaluate the safety of the Cardioband system in the post-marketing setting.

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