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Getinge's Beating Heart Product Family Post-Market Clinical Follow-up (PMCF) Study

Getinge's Beating Heart Product Family Post-Market Clinical Follow-up (PMCF) Study

Recruiting
22 years and older
All
Phase N/A

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Overview

This observational study aims to collect data on the performance and safety of Getinge's Beating Heart products used during open-heart coronary artery bypass graft surgery. The surgery and the use of the study devices will be done according to the standard of care. Participants will not be required to undergo any study-specific procedures, and information will be collected only until hospital discharge following the surgery.

Eligibility

Inclusion Criteria:

  • ≥ 22 years of age
  • Patient (or a legally authorized representative) is willing and able to provide signed informed consent, if required
  • Undergoing planned beating heart coronary artery bypass graft procedure with/without left atrial appendage closure, where the use of at least one Getinge's Beating Heart study product is anticipated.

Exclusion Criteria:

  • Patients undergoing heart valve surgery
  • Patients who undergo either planned or unplanned conversion to on pump with arrested heart where Getinge's Beating Heart product(s) have not been used.

Study details
    Off Pump Coronary Artery Bypass Surgery

NCT07286890

Maquet Cardiovascular

13 May 2026

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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