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Study identifier: NCT05298124 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Transcatheter Mitral Valve Repair for Inotrope Dependent Cardiogenic Shock

Condition: Cardiogenic Shock · Mitral Regurgitation  ·  Sponsor: Ottawa Heart Institute Research Corporation

PhaseNA
Planned participants144
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Mitral regurgitation may be seen in the setting of cardiogenic shock. Transcatheter edge-to-edge repair (TEER) has been shown to improve outcomes in patients with chronic heart failure. Observational studies suggest improvements in clinical outcomes in patients with mitral regurgitation in the setting of cardiogenic shock; however, there remains a lack of randomized clinical data to support the use of TEER in cardiogenic shock. This study will be a multicenter, open-label, randomized-controlled trial with two study arms: medical therapy and TEER. Patients admitted to the Cardiac Intensive Care Unit (CICU), Cardiac Surgery Intensive Care Unit (CSICU) or Intensive Care Units (ICU) at participating centers will be recruited. The study aims to answer the question: "Does TEER in patients with SCAI stage C or D cardiogenic with concomitant moderate or greater mitral regurgitation improve outcomes as compared to medical therapy?" The study hypothesis is that TEER will lead to an overall improvement in the composite outcome as compared to the medical therapy arm.

This description comes directly from the study's public registry record.

Talk to the study team

Benjamin Hibbert, MD PhD  ·  613-696-7115  ·  bhibbert@ottawaheart.ca

Pietro Di Santo, MD  ·  613-696-7000  ·  pdisanto@ottawaheart.ca

Always discuss trial participation with your own doctor first.

Locations (4)

Mayo ClinicRochester, Minnesota, United StatesRecruiting
University of Ottawa Heart InstituteOttawa, Ontario, CanadaRecruiting
Sunnybrook HospitalToronto, Ontario, CanadaNot Yet Recruiting
St. Michael's HospitalToronto, Ontario, CanadaNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT05298124