Transcatheter Mitral Valve Repair for Inotrope Dependent Cardiogenic Shock

Not Applicable

Recruiting

Conditions: Cardiogenic Shock
Mitral Regurgitation

Interventions: Device: Transcatheter edge-to-edge repair
Other: Medical therapy

Registration Number: NCT05298124

Lead Sponsor: Ottawa Heart Institute Research Corporation

Brief Summary: 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.

Detailed Description: Current management strategies for patients with SCAI stage C through E cardiogenic shock include management in a cardiac intensive care unit (CICU) or cardiac surgery intensive care unit (CSICU) with intravenous inotropes (i.e. medications to increase the pumping function of the heart), vasopressors (i.e. medications to increase blood pressure), ventilatory support, and/or mechanical circulatory support. Importantly, with the exception of revascularization, little data exists demonstrating the ability to alter prognosis in patients with cardiogenic shock.

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 divided into two phases, as follows:

Phase 1 (Vanguard) - The first phase of this study will be composed of a feasibility stage where a total of 10 participants from centers in Ontario, Canada will be recruited. The primary objective of this phase is to ascertain feasibility of participant recruitment and treatment. Feasibility would be considered met if 10 participants were enrolled 12 months from the date of activation of all four centers.

Phase 2 - The second phase of this study will be a continuation of Phase 1 where the remaining 134 participants, for a total of 144 participants in the overall study. For this second phase of the study, patients will be recruited from high-volume TEER centers in Canada and the United States - with participating centers performing more than 25 TEER procedures per year.

Eligible participants will be randomly assigned in a 1:1 fashion to the medical therapy arm (i.e. control arm) or the TEER arm (i.e. intervention arm) of the trial.

Recruitment & Eligibility

Status: RECRUITING

Sex: All

Target Recruitment: 144

Inclusion Criteria

Participants or substitute decision maker is able and willing to provide written informed consent
Age ≥ 18 years
SCAI stage C or D cardiogenic shock with persistent inotrope/vasopressor/non-durable mechanical support or unable to wean ventilatory support due to pulmonary edema for 24 hours prior to randomization
Greater than or equal to 3+ MR as determined by a study center's transesophageal echocardiogram (TEE)
In the opinion of the study center's heart team the participant is anatomically eligible for TMVr with the potential to achieve <3+ MR

Exclusion Criteria

Unwilling or unable to obtain informed consent from the participant or substitute decision maker
Revascularization of coronary artery disease performed in the 48 hours prior to randomization
If the mechanism of MR is deemed to be degenerative, in the opinion of the heart team the participant is eligible for surgical intervention
Prior mitral valve leaflet surgery or implanted mitral valve prosthesis (excluding ring)
Echocardiographic evidence of left sided intracardiac mass or thrombus
Diagnosis of active infective endocarditis
Transesophageal echocardiogram is contraindicated
Mitral valve anatomy deemed contraindication to TMVr implantation that cannot be addressed procedurally as determined by the study center's heart team
Any aortic valve disease greater than moderate in severity
A known hypersensitivity or contraindication to procedure medications which cannot be adequately managed medically
Out of hospital cardiac arrest or in-hospital cardiac arrest without documented neurologic recovery
Plan for durable mechanical circulatory support implantation prior to TMVr
In the opinion of the treating team, there is a significant comorbidity that would limit life expectancy in hospital
Pregnant or planning to become pregnant in the next 6 months.

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Transcatheter edge-to-edge repair	Transcatheter edge-to-edge repair	The experimental arm includes treatment in an intensive care unit with intravenous medications (e.g. vasopressors and inotropes), ventilatory support or mechanical circulatory support plus transcatheter edge-to-edge repair
Medical therapy	Medical therapy	Medical therapy includes treatment in an intensive care unit with intravenous medications (e.g. vasopressors and inotropes), ventilatory support or mechanical circulatory support.

Primary Outcome Measures

Name	Time	Method
Primary composite outcome	Through duration of hospitalization, generally up to 12 weeks following admission	The primary outcome in this clinical trial will be a composite of in-hospital all-cause mortality, cardiac transplantation, implantation of durable LVAD, or discharge on palliative inotropic therapy.

Secondary Outcome Measures

Name	Time	Method
Device success	At time of discharge from hospitalization, generally up to 12 weeks following admission	All of the following must be present: I. Absence of procedural mortality or stroke II. Proper placement and positioning of the device III. Freedom from unplanned surgical or interventional procedures related to the device or access procedure IV. Continued intended safety and performance of the device, including: A. No evidence of structural or functional failure B. No specific device-related technical failure issues and complications C. Reduction of mitral regurgitation to either optimal or acceptable levels without significant mitral stenosis, and with no greater than mild (1+) paravalvular mitral regurgitation (and without associated hemolysis)
Bleeding	Through duration of hospitalization, generally up to 12 weeks following admission	* Any intracranial bleeding (excluding microhemorrhages \<10 mm evident only on gradient-echo MRI) * Clinically overt signs of hemorrhage associated with a drop in hemoglobin of ≥5 g/dL or a ≥15% absolute decrease in hematocrit * Fatal bleeding (bleeding that directly results in death within 7 d)
Vascular access complications	Through duration of hospitalization, generally up to 12 weeks following admission	Access site-related arterial or venous injury or injury to surrounding structures
Discharge on inotropes	Through duration of hospitalization, generally up to 12 weeks following admission	Discharge from index hospitalization on palliative inotropic therapy
In hospital all-cause mortality	Through duration of hospitalization, generally up to 12 weeks following admission	Death from any cause
In hospital implantation of durable left-ventricular assist device or cardiac transplantation	Through duration of hospitalization, generally up to 12 weeks following admission	Implantation of durable left-ventricular assist device or cardiac transplantation
Stroke or transient ischemic attack	Through duration of hospitalization, generally up to 12 weeks following admission	Acute episode of a focal or global neurological deficit as determined by or in conjunction with the designated neurologist
Residual mitral regurgitation	Through duration of hospitalization, generally up to 12 weeks following admission	Severity of residual mitral regurgitation as assessed by the core lab on last available in hospital echocardiogram
Technical success	Measured at exit from procedure room, generally 2 hours after implant	All of the following must be present: I. Absence of procedural mortality II. Successful access, delivery, and retrieval of the device delivery system III. Successful deployment and correct positioning of the first intended device IV. Freedom from emergency surgery or reintervention related to the device or access procedure.
Cardiac structural complications	Through duration of hospitalization, generally up to 12 weeks following admission	Cardiac perforation or pseudoaneurysm

Trial Locations

Locations (4): University of Ottawa Heart Institute
🇨🇦
Ottawa, Ontario, Canada
St. Michael's Hospital
🇨🇦
Toronto, Ontario, Canada
Sunnybrook Hospital
🇨🇦
Toronto, Ontario, Canada
Mayo Clinic
🇺🇸
Rochester, Minnesota, United States

Transcatheter Mitral Valve Repair for Inotrope Dependent Cardiogenic Shock

Recruitment & Eligibility

Study & Design

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