Randomised Investigation of the MitraClip Device in Heart Failure: 2nd Trial in Patients With Clinically Significant Functional Mitral Regurgitation

University Medical Center Goettingen35 sites in 9 countries505 target enrollmentMarch 2015

ConditionsMitral Valve Insufficiency

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Mitral Valve Insufficiency
Sponsor: University Medical Center Goettingen
Enrollment: 505
Locations: 35
Primary Endpoint: Rate of total (first and recurrent) HF hospitalizations within 24 months
Status: Completed
Last Updated: last year

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

To study the safety and effectiveness of the MitraClip System in the treatment of clinically significant functional mitral regurgitation in patients with New York Heart Association (NYHA) Functional Class II to Class IV chronic heart failure.

Detailed Description

The trial is designed to provide additional evidence regarding appropriate recommendations for use of the MitraClip System for patients with chronic heart failure and clinically significant functional mitral regurgitation. Additionally, the trial will collect evidence regarding health economics of the MitraClip System for use in this patient population.

Registry

clinicaltrials.gov

Start Date

March 2015

End Date

April 19, 2024

Last Updated

last year

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

University Medical Center Goettingen

Responsible Party

Principal Investigator

Karsten Gavenis

on behalf of Principle Investigator Prof. Wolfgang Schillinger and Prof. Stefan D. Anker

University Medical Center Goettingen

Eligibility Criteria

Inclusion Criteria

•Clinically significant functional mitral regurgitation (moderate-to-severe or severe MR) as defined by European Association of Echocardiography, within 90 days prior to randomization and confirmed by the Echocardiography Core Laboratory Note: The TTE must be obtained after the subject has been stabilized on optimal therapy and has undergone revascularization and/or CRT, as appropriate
•Assessed by the investigator to be on optimal standard of care therapy for heart failure, according to current ESC/HFA guidelines with no dose changes of heart failure drugs (with the exception of diuretics) during the last 2 weeks immediately prior to randomization.
•Symptomatic with documented New York Heart Association Class II, III or IV heart failure, despite optimal standard of care therapy, within 30 days preceding randomization
•Minimum of one documented hospitalization (acute care admission or emergency room visit) for heart failure within 12 months preceding randomization OR values of 300 pg/mL for BNP or 1000 pg/mL for NT-proBNP after optimal medical and/or device management within 90 days preceding randomization Note: BNP or NT-proBNP must be obtained after the subject has been stabilized on optimal therapy and has undergone revascularization and/or CRT, as appropriate
•Ambulatory patient with symptomatic congestive heart failure (CHF) in NYHA functional class II to IV (despite optimal standard of care therapy as assessed within 30 days preceding randomization) and with LVEF 20% to 50%. Note: LVEF needs to be determined by one of the following methods: transthoracic echocardiography (TTE), contrast ventriculography, gated blood pool scan, cardiac magnetic resonance) within 90 days prior to randomization
•Patient is ambulatory and able to perform a 6MWT with the only limiting factor(s) being due to cardiovascular fitness

Exclusion Criteria

•Mitral regurgitation is primarily due to degenerative disease of the mitral valve apparatus (Degenerative MR) as determined by transesophageal echocardiography (TEE).
•Status 1 heart transplant or prior orthotropic heart transplantation.
•Introduction of a new heart failure drug class within the last 2 weeks prior to randomization.
•Evidence of acute coronary syndrome, transient ischemic attack or stroke within 90 days prior to randomization. Note:Acute coronary syndrome (ACS) is defined as an ACS that requires an intervention. Increased troponin without acute symptoms and chest pain is not defined as ACS.
•Any percutaneous cardiovascular intervention, carotid surgery, cardiovascular surgery, or atrial fibrillation ablation within 90 days prior to randomization.
•Therapy with or without cardioverter-defibrillator (CRT or CRT-D), or Implantable Cardioverter Defibrillator (ICD)) within 90 day prior to randomization, or revision of any implanted rhythm management device within 90 days prior to randomization.
•Need for any cardiovascular surgery.
•Mitral valve surgery is considered the preferred therapeutic option for the subject
•Renal replacement therapy
•6-Minute Walk Test (6MWT) distance \> 475 meters

Outcomes

Primary Outcomes

Rate of total (first and recurrent) HF hospitalizations within 24 months

Time Frame: 24 months

Rate of total (first and recurrent) HF hospitalizations within 24 months

Composite rate of recurrent heart failure hospitalizations and cardiovascular (CV) death within 24 months

Time Frame: 24 months

Composite rate of recurrent heart failure hospitalizations and cardiovascular (CV) death within 24 months

Change in quality of life (i.e. overall KCCQ score) from baseline to 12 months

Time Frame: 12 months

Change in quality of life (i.e. overall KCCQ score) from baseline to 12 months

Secondary Outcomes

Rate of total (first and recurrent) hospitalizations for any cause within 24 months(24 months)
Percentage of patients in NYHA function class I/II at 12 months(12 months)
Change in 6 Minute Walking Test distance from baseline to 12 months(from baseline to 12 months)
Percentage of patients with mitral regurgitation grade of 2+ or lower at 12 months as assessed by the Echocardiography Core Laboratory(at 12 months)
All-cause mortality during all available follow-up(during all available follow-up)