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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03113552
Acronym
IPPVM
Enrollment
1500
Registered
2017-04-13
Start date
2013-02-04
Completion date
2028-07-04
Last updated
2023-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mitral Plasty, Mitral Valve Prolapse

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.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Survival defines as the time between the date of surgery and the death or date of the last news6 months

Countries

France

Contacts

Primary ContactCatherine SZYMANSKI, Dr
szymanski.catherine@chu-amiens.fr+33322455885

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026