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Clinical Trials/NCT03113552
NCT03113552
Recruiting
Not Applicable

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

Centre Hospitalier Universitaire, Amiens1 site in 1 country1,500 target enrollmentFebruary 4, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mitral Valve Prolapse
Sponsor
Centre Hospitalier Universitaire, Amiens
Enrollment
1500
Locations
1
Primary Endpoint
Survival defines as the time between the date of surgery and the death or date of the last news
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
February 4, 2013
End Date
July 4, 2028
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients operated between 1988 and 2011
  • Presence of a valvular prolapse diagnosed by echocardiography
  • Possibility of a complete clinical evaluation at the time of the initial echocardiography

Exclusion Criteria

  • Ischemic MI (including papillary muscle rupture)
  • Presence of significant aortic valvulopathy, mitral valvular stenosis or congenital disease
  • History of cardiac surgery

Outcomes

Primary Outcomes

Survival defines as the time between the date of surgery and the death or date of the last news

Time Frame: 6 months

Study Sites (1)

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