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OpenTrials
Completed

NCT Number: NCT00394797

Surgical Correction of Moderate Ischemic Mitral Regurgitation

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Shaare Zedek Medical Center

Jerusalem, 91031, Israel

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

mitral valve annuloplasty

Procedure

Primary outcomes

  1. survival at 1,5 and 10 years

Secondary outcomes

  1. event free survival

  2. symptoms

  3. echocardiographic parameters

Sponsors and collaborators

Lead sponsor

Shaare Zedek Medical Center

Other

Registry information

Important dates

First posted
Nov 1, 2006
Registry last updated
Jun 1, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.