Actively Recruiting
Percutaneous Coronary RevascularizatiOn VERsus Coronary-Artery Bypass Grafting for Multivessel Disease in Patients With Left Ventricular Dysfunction (PROVERB)
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2023-03-22
1040
Participants Needed
1
Research Sites
539 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A short description, 5000 characters Ischemic cardiomyopathy related to coronary artery disease is currently the leading cause of heart failure. When it is responsible for heart failure, the coronary artery disease likely involves 2 or 3 vessels. Percutaneous coronary angioplasty, which is the other available technique for coronary revascularization, has never been evaluated in this indication. The results of retrospective registries studying the strategy for multivessel revascularization in patients with heart failure are inconsistent and no randomized study has been performed so far. Currently, ESC guidelines recommends to perform coronary-artery bypass grafting (IB) or percutaneous coronary intervention (IIa C) with the acknowledgement that percutaneous coronary intervention has never been properly evaluated in this setting. However, it has been previously demonstrated that left ventricle dysfunction significantly increases mortality and morbidity during and after cardiac surgery (3-10% mortality when LVEF is ≤30%). Moreover, the technical progresses in stent development and manufacturing have led to a dramatic decrease in the incidence of stent thrombosis and in-stent restenosis. Therefore, we hypothesize that percutaneous coronary angioplasty may be an attractive strategy for revascularization in patients with multi-vessel disease and left ventricle dysfunction, who are at high risk of surgical complication. Thus, we aim to test the hypothesis that percutaneous coronary intervention is non-inferior to coronary-artery bypass grafting for revascularization in patients with multivessel disease and left ventricle dysfunction. The main objective is to demonstrate that percutaneous coronary angioplasty is non-inferior to coronary-artery bypass grafting for multivessel revascularization in patients with left ventricular dysfunction on major cardiac and cerebrovascular events (MACCE). Method:A Prospective Randomized Open label, Blinded Endpoint, parallel-group, active controlled, non-inferiority, multicenter trial.
CONDITIONS
Official Title
Percutaneous Coronary RevascularizatiOn VERsus Coronary-Artery Bypass Grafting for Multivessel Disease in Patients With Left Ventricular Dysfunction (PROVERB)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Left ventricle ejection fraction 35% or less measured by echocardiography, cardiac magnetic resonance imaging ventriculogram, or gated Single Photon Emission Computed Tomography ventriculogram
- Multivessel disease suitable for revascularization, including three vessel disease or two vessel disease involving left main or proximal left anterior descending artery
- Clinical and anatomic eligibility for both percutaneous coronary intervention and coronary artery bypass grafting as agreed by the local Heart Team
- Ability to sign informed consent and comply with all study procedures, including follow-up for at least two years
- Affiliation to health insurance
You will not qualify if you...
- Prior percutaneous coronary intervention of any coronary artery lesions within 6 months before randomization
- Prior coronary artery bypass grafting at any time before randomization
- Ongoing cardiogenic shock at the time of coronary angiogram (systolic blood pressure less than 90 mmHg with clinical signs of low output or need for inotropic agents)
- Contraindication for PCI or CABG determined by the heart team
- Indication for another cardiac surgery if CABG is performed
- ST elevation myocardial infarction within 30 days
- Non-cardiac illness with life expectancy less than 24 months
- Current participation in other investigational drug or device studies
- Women who are pregnant or nursing
- Females of childbearing potential without effective birth control
- Patients under tutorship or curatorship
- Patients receiving state medical aid (AME)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Assistance Publique Hôpitaux de Paris - CHU HENRI MONDOR
Créteil, Val De Marne, France, 94000
Actively Recruiting
Research Team
R
Romain GALLET, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here