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Surgical Correction of Moderate Ischemic Mitral Regurgitation

NCT ID: NCT00394797

Last Updated: 2011-06-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Study Classification

OBSERVATIONAL

Brief Summary

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The purpose of this study is to try and determine whether repair of moderate ischemic mitral regurgitation at the time of coronary bypass graft surgery (CABG) has an impact on survival.We will compare patients undergoing CABG + mitral repair or CABG only groups. Primary endpoints include late survival. Secondary endpoints include event free survival, symptoms, and echocardiographic outcomes.

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Detailed Description

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Conditions

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Moderate Ischemic Mitral Regurgitation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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mitral valve annuloplasty

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patients undergoing coronary bypass surgery who have moderate degree of ischemic MR

Exclusion Criteria

* etiology of mitral regurgitation other than ischemic, degree of regurgitation other than moderate.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shaare Zedek Medical Center

OTHER

Sponsor Role lead

Principal Investigators

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Shuli Silberman, MD

Role: PRINCIPAL_INVESTIGATOR

Shaare Zedek Medical Center

Locations

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Shaare Zedek Medical Center

Jerusalem, , Israel

Site Status

Countries

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Israel

Other Identifiers

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IMR001

Identifier Type: -

Identifier Source: org_study_id

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