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NCT Number: NCT06930092

RestoratIon of Myocardial Function by PeRcutaneous cOronary interVEntion in Patients With Ischemic CardioMyoPathy

To compare the effects of physiology- and imaging-guided PCI combined with optimal medical therapy (OMT) versus OMT alone on the recovery of left ventricular systolic function in patients with ischemic cardiomyopathy and multivessel coronary artery disease.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

This study is a prospective, open-label, randomized, multicenter trial to test the safety and efficacy of physiology- and imaging-guided complete revascularization with PCI combined with optimal medical therapy (OMT) versus OMT alone on the recovery of left ventricle ejection fraction (LVEF) in patients with ischemic cardiomyopathy and multivessel coronary artery disease.

The primary hypothesis is that physiology- and imaging-guided complete revascularization with PCI combined with OMT will show greater improvements in LV systolic function at 6 months after randomization compared with OMT alone.

Patients with left ventricular ejection fraction (LVEF) less than 40% on echocardiography will undergo gadolinium-enhanced cardiac MRI to determine the underlying cause of cardiac dysfunction and assess the presence of viable myocardium. Among patients suspected of having ischemic cardiomyopathy, those who provide informed consent will be considered for enrollment. Eligible patients undergoing invasive coronary angiography and meeting inclusion and exclusion criteria will be randomly assigned to either: a group receiving physiology- and imaging-guided PCI in combination with optimal medical therapy, or a group receiving optimal medical therapy alone.

Improvement in LVEF will be evaluated using follow-up gadolinium-enhanced cardiac MRI at 6 months. Clinical outcomes will be assessed at 6 and 12 months, and long-term outcomes will be analyzed through 36-month follow-up.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject must be ≥ 19 years
  • Subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of receiving invasive physiologic or imaging evaluation and PCI and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
  • Subject with LV ejection fraction <40% from cardiac MRI
  • Subject with multivessel disease in major epicardial coronary artery disease or their major branches (vessel size of 2.5 mm or more than 2.5mm) considering coronary revascularization

Exclusion criteria

  • Subjects with more than 50% transmural extent of infarction on GE-MRI in more than 25% of the dysfunctional myocardial segments
  • Subject with suspicious of other cardiomyopathy (dilated cardiomyopathy, hypertrophic cardiomyopathy etc.)
  • Subject with recent myocardial infarction within 4 weeks
  • Subject with recent fatal arrhythmia (VT or VF) within 4 weeks
  • Subject with hemodynamically unstable state
  • Subject with complex coronary artery lesions, such as chronic total occlusions, in which complete revascularization is considered unfeasible
  • Subject for whom coronary artery bypass surgery is prioritized over coronary artery intervention
  • Subject with severe valvular heart disease requiring open heart surgery
  • Subject with history of coronary artery bypass surgery or valve surgery
  • Subject with expected life expectancy of less than 1 year
  • Subject considered ineligible for this study based on the investigator's discretion

Treatment and study plan

Physiology-and imaging-guided PCI

Procedure

The criteria for performing revascularization are as follows

  • Lesions with ≥50% diameter stenosis and FFR ≤ 0.80, or lesions with severe stenosis (>90%)
  • In vessels meeting the above criteria, IVUS findings consistent with either:
  • Minimum lumen area (MLA) ≤ 3 mm²
  • 3 mm² < MLA ≤ 4 mm² and plaque burden >70%

For all target vessels and lesions identified for intervention, optimal revascularization should be pursued. The criteria for optimal revascularization are as follows, and operators are encouraged to achieve them:

  • Post-PCI FFR > 0.86 in all treated vessels is recommended, with a minimum threshold of post-PCI FFR > 0.80 to achieve functional complete revascularization.
  • Post-PCI ΔFFR (defined as [FFR at stent distal edge] - [FFR at stent proximal edge]) < 0.05 is recommended.
  • On IVUS, achieving a minimum stent area (MSA) > 5.5 mm² and MSA/average reference lumen > 80% is recommended.

Optimal medical treatment

Drug

All study participants will receive guideline-directed medical therapy. Even for patients assigned to the optimal medical therapy group, revascularization may be performed during follow-up if clinically indicated. If such a decision is made prior to the primary endpoint assessment, a gadolinium-enhanced cardiac MRI will be performed at the time of consideration to reassess myocardial viability.

Primary outcomes

  1. LV ejection fraction from GE-MRI

    Time frame: At 6 months after randomization

    LV ejection fraction from gadolinium-enhanced MRI

Secondary outcomes

  1. Changes in the transmural extent of myocardial infarction from GE-MRI

    Time frame: At 6 months after randomization

    Changes in the transmural extent of myocardial infarction from GE-MRI

  2. Number of improved dysfunctional myocardial segments from GE-MRI

    Time frame: At 6 months after randomization

    Number of improved dysfunctional myocardial segments from GE-MRI

  3. Changes in the LV chamber size from GE MRI

    Time frame: At 6 months after randomization

    Changes in the LV chamber size from GE MRI

  4. LV ejection fraction from echocardiography

    Time frame: At 6 months and 12 months after randomization

    LV ejection fraction from echocardiography

  5. Number of improved dysfunctional myocardial segments from echocardiography

    Time frame: At 6 months and 12 months after randomization

    Number of improved dysfunctional myocardial segments from echocardiography

  6. Changes in the LV chamber size change from echocardiography

    Time frame: At 6 months and 12 months after randomization

    Changes in the LV chamber size change from echocardiography

  7. All-cause death

    Time frame: At 6 months, 12 months, and 36 months after randomization

    death from any cause

  8. Cardiovascular death

    Time frame: At 6 months, 12 months, and 36 months after randomization

    death from cardiovascular cause

  9. Non-fatal myocardial infarction

    Time frame: At 6 months, 12 months, and 36 months after randomization

    Non-fatal myocardial infarction

  10. Unplanned revascularization

    Time frame: At 6 months, 12 months, and 36 months after randomization

    Unplanned revascularization

  11. Hospitalization for heart failure

    Time frame: At 6 months, 12 months, and 36 months after randomization

    Hospitalization for heart failure

  12. EuroQol 5-Dimension 5-Level Questionnaire

    Time frame: At 6 months, 12 months, and 36 months after randomization

    EuroQol 5-Dimension 5-Level Questionnaire

  13. Brain natriuretic peptide (BNP or NT-Pro BNP) level

    Time frame: At 6 months, 12 months, and 36 months after randomization

    Brain natriuretic peptide (BNP or NT-Pro BNP) level

Study contacts

Contact information is provided by the study sponsor or research team.

Doyeon Hwang, MD

CONTACT

[email protected]

82-10-7446-2779

Junpil Yun, MD

CONTACT

[email protected]

82-10-8001-9969

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Collaborators

  • Seoul National University Boramae Hospital
  • Seoul National University Bundang Hospital

Registry information

Acronym: IMPROVE-ICMP

Important dates

Study start
2025
Primary completion
2028
Study completion
2029
First posted
Apr 16, 2025
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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