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OpenTrials
Completed

NCT Number: NCT06766123

Outcomes of Coronary Artery Bypass Grafting in Israeli Jews and Arabs

Retrospective study of adult patients with multivessel disease undergoing isolated CABG in three centers between January 1st, 2009, and December 31st, 2023. The primary outcome was a composite of major adverse cardiac and cerebrovascular events (MACCE). Patients were grouped according to their ethnic origin, Arabs and Jews.

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Key information

Conditions

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • isolated CABG

Exclusion criteria

  • members of different HMO

Treatment and study plan

CABG

Procedure

All patients underwent isolated CABG and retrospectively followed to asses ethnic disparities

Primary outcomes

  1. MACCE

    Time frame: through study completion, a median of 78 months

Secondary outcomes

  1. Mortality

    Time frame: through study completion, a median of 78 months

  2. MI

    Time frame: through study completion, a median of 78 months

  3. CVA

    Time frame: through study completion, a median of 78 months

  4. repeat revascularization

    Time frame: through study completion, a median of 78 months

  5. utilization of multi-arterial grafting

    Time frame: through study completion, a median of 78 months

Sponsors and collaborators

Lead sponsor

Technion, Israel Institute of Technology

Other

Registry information

Important dates

Study start
2009
Primary completion
2023
Study completion
2023
First posted
Jan 9, 2025
Registry last updated
Jan 9, 2025

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.

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