Seoul National University Hospital
Seoul, Chongno-gu, 03080, South Korea
Location status: Recruiting
Location contact
Doyeon Hwang, MD
CONTACT
Junpil Yun, MD
CONTACT
NCT Number: NCT06930092
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.
Interested in participating?
Request Info19 year and older
All sexes
Interventional
Not applicable
Seoul, Chongno-gu, 03080, South Korea
Location status: Recruiting
Doyeon Hwang, MD
CONTACT
Junpil Yun, MD
CONTACT
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The criteria for performing revascularization are as follows
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:
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.
Time frame: At 6 months after randomization
LV ejection fraction from gadolinium-enhanced MRI
Time frame: At 6 months after randomization
Changes in the transmural extent of myocardial infarction from GE-MRI
Time frame: At 6 months after randomization
Number of improved dysfunctional myocardial segments from GE-MRI
Time frame: At 6 months after randomization
Changes in the LV chamber size from GE MRI
Time frame: At 6 months and 12 months after randomization
LV ejection fraction from echocardiography
Time frame: At 6 months and 12 months after randomization
Number of improved dysfunctional myocardial segments from echocardiography
Time frame: At 6 months and 12 months after randomization
Changes in the LV chamber size change from echocardiography
Time frame: At 6 months, 12 months, and 36 months after randomization
death from any cause
Time frame: At 6 months, 12 months, and 36 months after randomization
death from cardiovascular cause
Time frame: At 6 months, 12 months, and 36 months after randomization
Non-fatal myocardial infarction
Time frame: At 6 months, 12 months, and 36 months after randomization
Unplanned revascularization
Time frame: At 6 months, 12 months, and 36 months after randomization
Hospitalization for heart failure
Time frame: At 6 months, 12 months, and 36 months after randomization
EuroQol 5-Dimension 5-Level Questionnaire
Time frame: At 6 months, 12 months, and 36 months after randomization
Brain natriuretic peptide (BNP or NT-Pro BNP) level
Contact information is provided by the study sponsor or research team.
Doyeon Hwang, MD
CONTACT
Junpil Yun, MD
CONTACT
Seoul National University Hospital
Other
Acronym: IMPROVE-ICMP
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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