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Mitral Valve Prolapse clinical trials

View clinical trials related to Mitral Valve Prolapse.

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NCT ID: NCT03113552 Recruiting - Clinical trials for Mitral Valve Prolapse

Prognostic Impact of the Location of Mitral Valve Prolapse on the Long-term Results of Mitral Plasty

IPPVM
Start date: February 4, 2013
Phase:
Study type: Observational

Mitral insufficiency (MI) accounts for 24% of adult valvulopathies and affects 7% of subjects older than 75 years. They are the second leading cause of valvulopathy in Europe. The most common etiology is the associated valvular prolapse. Mitral surgery remains the reference treatment for symptomatic MI. The success of this procedure depends on the mitral valve geometry and the location of the prolapse. The site of the prolapse, whether monovalvular, localized to the posterior or anterior leaflet, or bivalvular, influences the possibilities and probably the long-term results of the plasty.

NCT ID: NCT02552771 Recruiting - Clinical trials for Mitral Valve Prolapse

The Canadian Mitral Research Alliance (CAMRA) Trial CardioLink-2

CAMRA
Start date: January 2016
Phase: N/A
Study type: Interventional

Multicentre, double-armed, randomized controlled trial designed to compare mitral valve leaflet resection versus leaflet preservation with regards to the development of functional mitral stenosis following surgical repair of mitral valve prolapse. Patients will be randomized (1:1) to receive: (1) mitral valve repair with a leaflet resection or (2) mitral valve repair with leaflet preservation (using polytetrafluoroethylene neochordae), followed by echocardiographic and clinical assessment at 12-months following surgery.

NCT ID: NCT01719211 Recruiting - Clinical trials for Mitral Valve Prolapse

Genetic Basis of Mitral Valve Prolapse

MVP
Start date: January 1999
Phase:
Study type: Observational

The investigators have successfully identified two novel genetic loci for MVP on chromosomes 11 and 13 and are searching for altered genes in these regions. This requires recruiting large families who may have MVP linked to these or other chromosomes; and obtaining DNA samples from 1,000-1,500 individually affected patients to study the relation between DNA markers throughout the genome and MVP. It is our expectation that the results of this study will lead to the discovery of gene(s) responsible for MVP. This will lead to improved understanding of the disease and, in turn, improved ability to treat and prevent progression in genetically susceptible individuals.