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Revascularization Versus Medical Treatment in Patients With Ischemic Left Ventricular Dysfunction

Randomized Controlled Trial of Revascularization Versus Medical Treatment on Clinical Outcomes in Patients With Reduced Left Ventricular Function

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05828719
Acronym
RESTORE-PCI
Enrollment
900
Registered
2023-04-25
Start date
2023-06-16
Completion date
2030-12-31
Last updated
2025-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure With Reduced Ejection Fraction, Ischemic Cardiomyopathy

Keywords

ischemic cardiomyopathy, percutaneous coronary intervention, ejection fraction, guideline-directed medical treatment

Brief summary

Randomized trial to compare clinical outcomes between revascularization versus medical treatment alone in patients with ischemic cardiomyopathy and left ventricular dysfunction.

Detailed description

Ischemic cardiomyopathy, the term used to describe systolic dysfunction due to chronic myocardial ischemia from ischemic heart disease, is the most common form of heart failure. To adapt to this ischemic environment, myocardium is known to undergo downregulation that may revert after adequate perfusion is re-established, a phenomenon known as myocardium hibernation. This phenomenon has been a background for the main concept of management for ischemic cardiomyopathy via revascularization. Indeed, the recent 10-year follow-up reports from STICH trial demonstrated improved long-term clinical outcomes after coronary bypass graft surgery than optimal medical therapy (OMT) in patients with ischemic cardiomyopathy. Percutaneous coronary intervention (PCI) is another intervention that is commonly used to revascularize significant coronary stenosis. Despite common belief that revascularization by PCI would improve perfusion to ischemic myocardium and improve clinical outcomes, several clinical trials have failed to show beneficial impact of PCI over OMT in stable ischemic heart disease other than symptomatic improvement. Recently published REVIVED trial compared effect of PCI and OMT in ischemic cardiomyopathy patients with left ventricular ejection fraction \< 35% and demonstrable viable myocardial segments, and found no significant difference in clinical outcomes of both groups. However, whether PCI optimized by additional information can make a difference in this setting remains unanswered. It is known that intravascular imaging and coronary physiologic testing using intravascular ultrasound (IVUS), optical coherence tomography (OCT) or fractional flow reserve (FFR) result in better outcomes compared to conventional angiography alone. IVUS provides anatomical information regarding the lumen, plaque, and plaque characteristics, and can optimize stent placement minimizing stent-related problems and lead to better outcomes. On the other hand, FFR provides information on amount of ischemia which the stenosis in question is causing, and also improves the quality of PCI which has been demonstrated by multiple previous trials. Unfortunately, proportion of IVUS and FFR use is not disclosed in REVIVED trial, and it is possible there is a room for improvement if the PCI is further guided by these adjunctive diagnostic procedures in regard to the clinical outcomes. In this regard, it is our hypothesis that PCI guided and optimized by intravascular imaging and FFR-guided strategy would bring additional benefit that may result in significant difference of prognosis for ischemic cardiomyopathy compared to OMT alone. Randomized controlled trial to test this hypothesis would provide valuable evidence to guide treatment strategy for ischemic cardiomyopathy. Therefore, RESTORE-PCI trial has been designed to compare clinical outcomes after state-of-the-art PCI or OMT for ischemic cardiomyopathy. The aim of the study is to compare clinical outcomes between revascularization versus medical treatment alone in patients with ischemic cardiomyopathy and left ventricular dysfunction. Primary hypothesis is that revascularization guided by invasive physiologic indexes and optimized by intravascular imaging device plus optimal medical treatment (OMT) would reduce risk of primary composite end point (major adverse cardiac events \[MACE\], a composite of death, myocardial infarction (MI), admission for heart failure, or advanced heart failure requiring LVAD or transplantation) than OMT alone in patients with ischemic cardiomyopathy.

Interventions

PROCEDUREPercutaneous coronary intervention

Revascularization indication 1. Diameter stenosis \>90% by visual assessment 2. Functionally significant stenosis (FFR≤0.80 or non-hyperemic pressure ratios≤0.89) 3. Chronic total occlusion with substantial ischemic territory. The below locations will be judged as having substantial ischemic territory. * Left main artery * Proximal to mid left anterior descending artery * Proximal left circumflex artery in left dominant coronary arterial system * Proximal to distal right coronary artery in right dominant coronary arterial system

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Clinical outcome assessment will be performed under blinded assessment about the allocated treatment group.

Intervention model description

Prospective, multi-center, open-label, randomized controlled, superiority trial

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subject must be at least 19 years of age * Patients with stage C heart failure and left ventricular ejection fraction\<40% * Patients with significant coronary artery stenosis (diameter stenosis\>50% with proven inducible myocardial ischemia by invasive physiologic assessment) * Coronary artery disease is amenable for percutaneous coronary intervention (PCI) * Subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of receiving invasive approach and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.

Exclusion criteria

* Myocardial infarction by universal definition within 4 weeks of randomization * Non-viable myocardium in myocardial viability test (cardiac magnetic resonance, dobutamine-stress echocardiography, delayed single-photon emission computerized tomography, or aneurysmal change in echocardiography) * Target lesions not amenable for PCI by operators' decision * Patients who need left ventricular assisted device (LVAD) or heart transplantation at the time of randomization * Intolerance to Aspirin, Clopidogrel, Prasugrel, Ticagrelor, Heparin, or Everolimus * Known true anaphylaxis to contrast medium (not allergic reaction but anaphylactic shock) * Pregnancy or breast feeding * Non-cardiac co-morbid conditions are present with life expectancy \<2 year or that may result in protocol non-compliance (per site investigator's medical judgment) * Unwillingness or inability to comply with the procedures described in this protocol.

Design outcomes

Primary

MeasureTime frameDescription
major adverse cardiac events [MACE]2 years after last patient enrollmenta composite of death, myocardial infarction (MI), admission for heart failure, or advanced heart failure requiring LVAD or transplantation

Secondary

MeasureTime frameDescription
All-cause death2 years after last patient enrollmentAll-cause death
Cardiac death2 years after last patient enrollmentCardiac death
Any myocardial infarction2 years after last patient enrollmentAny myocardial infarction by Forth Universal definition of MI
Spontaneous myocardial infarction2 years after last patient enrollmentSpontaneous myocardial infarction by Forth Universal definition of MI
Procedure-related myocardial infarctionAfter index procedureProcedure-related myocardial infarction by ARC II definition
Advanced heart failure requiring LVAD or transplantation2 years after last patient enrollmentAdvanced heart failure requiring LVAD or transplantation
Admission for heart failure2 years after last patient enrollmentAdmission for acute decompensated heart failure
Clinically-indicated unplanned revascularization2 years after last patient enrollmentClinically-indicated unplanned revascularization
Stroke2 years after last patient enrollmentStroke (ischemic or hemorrhagic)
EQ-5D-5L (quality of life)at 6 month after index procedureEQ-5D-5L (quality of life)
SAQ (angina severity)at 6 month after index procedureSAQ (angina severity)
Left ventricular ejection fractionat 6 month - 1 year follow-up after index procedureLeft ventricular ejection fraction by echocardiography
NT-proBNPat 6 month - 1 year follow-up after index procedureNT-proBNP, pg/mL
Implantable cardioverter-defibrillator (ICD) or Cardiac resynchronization therapy (CRT-D)2 years after last patient enrollmentIncidence of Implantable cardioverter-defibrillator (ICD) or Cardiac resynchronization therapy (CRT-D) for documented ventricular tachycardia or ventricular fibrillation (secondary prevention).

Countries

South Korea

Contacts

Primary ContactYoung Bin Song, MD, PhD
youngbien.song@samsung.com82-2-3410-6653
Backup ContactJoo Myung Lee, MD, MPH, PhD
drone80@hanmail.net82-2-3410-3419

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026