ong-term follow-up after restrictive mitral annuloplasty for functional mitral regurgitation.

• Conditions: Mitral regurgitation; 10046973; 10007593

• Registration Number: NL-OMON42573
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 200

Inclusion Criteria

Patients who have undergone a restrictive mitral annuloplasty between the years 2000 and 2014 at the LUMC.

Exclusion Criteria

Patients in whom the restrictive annuloplasty ring has been explanted.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Cardiac mortality.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- All-cause mortality<br /><br>- Valve-related mortality<br /><br>- Hospital readmissions for heart failure and other cardiovascular causes<br /><br>- Major adverse valve-related events<br /><br>- Echocardiographic outcome (atrial and ventricular dimensions, volumes and<br /><br>function; mitral and tricuspid regurgitation, effective orifice area and<br /><br>transvalvular gradients)<br /><br>- Functional outcome (6-minute walk test, NYHA, CCS)<br /><br>- Quality of life (SF-36 questionnaire, Minnesota Living with Heart Failure<br /><br>Questionnaire)</p><br>