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Heart Failure With Reduced Ejection FractionRESTORE-PCINCT05828719

Revascularization Versus Medical Treatment in Patients With Ischemic Left Ventricular Dysfunction

A study testing Percutaneous coronary intervention in people with Heart Failure With Reduced Ejection Fraction and Ischemic Cardiomyopathy, run by Samsung Medical Center at 1 site in South Korea.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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

Who is it for?
Ages 19 years and older
What is being tested?
Percutaneous coronary intervention
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
900 participants
Where
1 siteSouth Korea
Study dates
16 Jun 2023to 31 Dec 2030
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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)
Show all 9Show fewer
  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Young Bin Song, MD, PhD contact

82-2-3410-6653

youngbien.song@samsung.com

Joo Myung Lee, MD, MPH, PhD contact

82-2-3410-3419

drone80@hanmail.net

South Korea1 site, 1 recruiting
  • Samsune Medical Center

    Seoul, 06351

    Young Bin Song, MD, PhD, 0234102575, youngbin.song@gmail.com

    Joo Myung Lee, MD, MPH, PhD, 0234102575, drone80@hanmail.net

    Recruiting

Other trials in South Korea

About this study

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

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

Read the 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.

Being tested
Percutaneous coronary intervention
Keywords
ischemic cardiomyopathy, percutaneous coronary intervention, ejection fraction, guideline-directed medical treatment

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Percutaneous coronary interventionProcedure or surgery

    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
Study groups in NCT05828719
Study groupRoleWhat they receive
Guideline-directed medical treatment groupNo interventionIn the GDMT group, medical treatment for patients with left ventricular dysfunction will be performed under current ACC/AHA/SCAI or ESC/EACTS guidelines for heart failure.
Revascularization groupExperimentalIn the revascularization group, patients will undergo percutaneous coronary intervention (PCI) using standard techniques under current ACC/AHA/SCAI or ESC/EACTS guidelines. In the revascularization group, the procedure must be within 2 weeks of randomization. Revascularization criteria is presented as below. 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
Receives: Procedure: Percutaneous coronary intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. major adverse cardiac events [MACE]

    a composite of death, myocardial infarction (MI), admission for heart failure, or advanced heart failure requiring LVAD or transplantation

    Measured: 2 years after last patient enrollment

Secondary outcomes (14)
  1. All-cause death

    All-cause death

    Measured: 2 years after last patient enrollment

  2. Cardiac death

    Cardiac death

    Measured: 2 years after last patient enrollment

  3. Any myocardial infarction

    Any myocardial infarction by Forth Universal definition of MI

    Measured: 2 years after last patient enrollment

  4. Spontaneous myocardial infarction

    Spontaneous myocardial infarction by Forth Universal definition of MI

    Measured: 2 years after last patient enrollment

  5. Procedure-related myocardial infarction

    Procedure-related myocardial infarction by ARC II definition

    Measured: After index procedure

  6. Admission for heart failure

    Admission for acute decompensated heart failure

    Measured: 2 years after last patient enrollment

  7. Advanced heart failure requiring LVAD or transplantation

    Advanced heart failure requiring LVAD or transplantation

    Measured: 2 years after last patient enrollment

  8. Implantable cardioverter-defibrillator (ICD) or Cardiac resynchronization therapy (CRT-D)

    Incidence of Implantable cardioverter-defibrillator (ICD) or Cardiac resynchronization therapy (CRT-D) for documented ventricular tachycardia or ventricular fibrillation (secondary prevention).

    Measured: 2 years after last patient enrollment

  9. Clinically-indicated unplanned revascularization

    Clinically-indicated unplanned revascularization

    Measured: 2 years after last patient enrollment

  10. Stroke

    Stroke (ischemic or hemorrhagic)

    Measured: 2 years after last patient enrollment

  11. EQ-5D-5L (quality of life)

    EQ-5D-5L (quality of life)

    Measured: at 6 month after index procedure

  12. SAQ (angina severity)

    SAQ (angina severity)

    Measured: at 6 month after index procedure

  13. Left ventricular ejection fraction

    Left ventricular ejection fraction by echocardiography

    Measured: at 6 month - 1 year follow-up after index procedure

  14. NT-proBNP

    NT-proBNP, pg/mL

    Measured: at 6 month - 1 year follow-up after index procedure

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Apr 2023
  2. Study start16 Jun 2023
  3. Primary completion1 Jul 2028 (estimated)
  4. Study completion31 Dec 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Prospective, multi-center, open-label, randomized controlled, superiority trial
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
900 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05828719
Sponsor's protocol ID
RESTORE119023
Acronym
RESTORE-PCI
Status last verified
Mar 2025
First submitted
12 Apr 2023
Last updated
14 Mar 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: After publication of first manuscript and trial results, the de-identified data will be shared by permission of principle investigator, when asked

Questions about this trial

What is this clinical trial studying?

A study testing Percutaneous coronary intervention in people with Heart Failure With Reduced Ejection Fraction and Ischemic Cardiomyopathy, run by Samsung Medical Center at 1 site in South Korea.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 14 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Young Bin Song, MD, PhD (82-2-3410-6653, youngbien.song@samsung.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

major adverse cardiac events [MACE] (time frame: 2 years after last patient enrollment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Mar 2025.

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