Ischemic Heart DiseaseSMART-CARENCT07009418
Smart Angioplasty Research Team-Coronary CT Angiography Versus Standard Care as Follow-up Strategies in High-Risk Patients After PCI (SMART-CARE)
A study testing Coronary CT Angiography (CCTA) in people with Ischemic Heart Disease and Coronary Artery Disease, run by Samsung Medical Center at 22 sites in South Korea.
Trial summary
The aim of the SMART-CARE trial is to compare clinical outcomes between coronary CT angiography (CCTA) versus standard care as follow-up strategies in high-risk patients after percutaneous coronary intervention (PCI). Read more about this study
- Who is it for?
- Ages 19 years and older
- Conditions the study is for
- Ischemic Heart Disease, Coronary Artery Disease
- What is being tested?
- Coronary CT Angiography (CCTA)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 3,500 participants
- Where
- 22 sitesSouth Korea
- Study dates
- 2 Oct 2025to 31 Dec 2032
- 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
- ① Patients aged 19 years old
- ② Patients who underwent successful PCI with one or more contemporary drug-eluting stents (stent diameter ≥3mm) or drug-coated balloons.
- ③ Patients must have at least one of the following criteria of complex coronary artery lesions or high-risk clinical characteristics:
- Complex coronary artery lesions:
- True bifurcation lesion (Medina 1,1,1/1,0,1/0,1,1) with side branch ≥2.5mm size ii. Chronic total occlusion (≥3 months) as target lesion iii. PCI for unprotected left main (LM) disease (LM ostium, body, distal LM bifurcation including non-true bifurcation) iv. Long coronary lesions (used stents or drug-coated balloons ≥38 mm in length) v. Multi-vessel PCI (≥2 major epicardial coronary arteries treated at one PCI session) vi. Multiple devices needed (≥3 more stents or drug-coated balloons per patient) vii. In-stent restenosis lesion as target lesion viii. Severely calcified lesion (encircling calcium in angiography) ix. Left anterior descending (LAD), left circumflex artery (LCX), and right coronary artery (RCA) ostial lesion
- High-risk clinical characteristics:
Show all 10Show fewer
- Acute myocardial infarction (ST-elevation myocardial infarction [MI] or non-ST-elevation MI) with or without cardiogenic shock (SCAI Classification ≥C) at presentation ii. Diabetes mellitus which requires medical treatment (oral hypoglycemic agents or insulin) iii. End-stage renal disease under dialysis iv. Combined vascular disease other than coronary artery disease
- Peripheral artery occlusive disease which is defined as A. Previous aorto-femoral bypass surgery, limb bypass surgery, or percutaneous transluminal angioplasty revascularization of the iliac, or infra-inguinal arteries, or B. Previous limb or foot amputation for arterial vascular disease, or C. History of intermittent claudication and one or more of the following: 1) An ankle/arm blood pressure (BP) ratio < 0.90, or 2) Significant peripheral artery stenosis (≥50%) documented by angiography, or by duplex ultrasound, or D. Previous carotid revascularization or asymptomatic carotid artery stenosis ≥50% as diagnosed by duplex ultrasound or angiography.
- Thoracoabdominal aortic disease which is defined as A. Documented thoracoabdominal aortic aneurysm by duplex ultrasound, angiography, or computed tomography angiography B. Previous endovascular or surgical treatment for thoracoabdominal aortic aneurysm
- ④ Subject who can verbally confirm understandings of risks, benefits and surveillance strategy alternatives of receiving CCTA and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
Who cannot join
- ① Advanced chronic kidney disease (Creatinine clearance <30 ml/min/1.73 m2) not on dialysis
- Known true anaphylaxis to contrast medium (not allergic reaction but anaphylactic shock)
- Pregnancy or breast feeding ④ Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment) ⑤ Unwillingness or inability to comply with the procedures described in this protocol.
Trial locations and contacts
22 sites in 1 country. Contact the study team or a site near you to ask about taking part.
22 sites in 1 country
South Korea22 sites, 22 recruiting
- Not yet recruiting
SoonChunHyang University Hospital Bucheon
Bucheon-si
Jon Suh, MD, PhD, marunada@gmail.com
Jon Suh, MD, PhD
- Not yet recruiting
Keimyung University Dongsan Medical Center
Daegu
Hyuck Jun Yoon, MD, PhD, hippsons@gmail.com
Hyuck Jun Yoon, MD, PhD
- Recruiting
Kyungpook National University Hospital
Daegu
Namkyun Kim, MD, PhD, namkyun.kim@knu.ac.kr
Namkyun Kim, MD, PhD
- Not yet recruiting
Chonnam National University Hospital, Chonnam National University Medical School
Gwangju
Seung Hun Lee, MD, PhD, lsh8602@naver.com
Young Joon Hong, MD, PhD, hyj200@hanmail.net
- Not yet recruiting
Chung-Ang University Gwangmyeong Hospital
Gwangmyeong
Jinhwan Jo, MD, PhD, jjh8732@gmail.com
Jinhwan Jo, MD, PhD
- Not yet recruiting
Inje University College of Medicine, Ilsan Paik Hospital
Ilsan
Sung Woo Cho, MD, PhD, drswcho@hanmail.net
Sung Woo Cho, MD, PhD
- Not yet recruiting
Gachon University Gil Medical Center
Incheon
Albert Youngwoo Jang, MD, PhD, albert.jang.md@gmail.com
Albert Youngwoo Jang, MD, PhD
- Not yet recruiting
Kwandong University Intl. ST. Mary's Hospital
Incheon
Hyung-Bok Park, MD, PhD, hyungbok7@gmail.com
Hyung-Bok Park, MD, PhD
- Not yet recruiting
Jeonbuk National University Hospital
Jeonju
Yisik Kim, MD, PhD, dr.kimesik@gmail.com
Yisik Kim, MD, PhD
- Not yet recruiting
Gyeongsang National University Hospital
Jinju
Jin Sin Koh, MD, PhD, kjs0175@gmail.com
Jin Sin Koh, MD, PhD
- Not yet recruiting
Seoul National University Bundang Hospital
Seongnam-si
Ki-Hyun Jeon, MD, PhD, imcardio@gmail.com
Ki-Hyun Jeon, MD, PhD
- Recruiting
Samsung Medical Center
Seoul, 06351
Joo Myung Lee, MD, MPH, PhD, 0234102575, drone80@hanmail.net
Joo Myung Lee, MD, MPH, PhD
- Not yet recruiting
Chung-Ang University Hospital, Chung-Ang University College of Medicine
Seoul
Kyung-Taek Park, MD, PhD, whgdkdy05@gmail.com
Kyung-Taek Park, MD, PhD
- Not yet recruiting
Ewha Womans University Seoul Hospital
Seoul
Sang Hoon Shin, MD, PhD, shin_sh@i.ewha.ac.kr
Sang Hoon Shin, MD, PhD
- Not yet recruiting
Hanyang University Seoul Hospital, College of Medicine, Hanyang University
Seoul
Young-Hyo Lim, MD, PhD, mdoim@hanyang.ac.kr
Young-Hyo Lim, MD, PhD
- Not yet recruiting
Korea University Anam Hospital
Seoul
Soon-Jun Hong, MD, PhD, psyche94@hanmail.net
Soon-Jun Hong, MD, PhD
- Not yet recruiting
Korea University Kuro Hospital
Seoul
Dong-Oh Kang, MD, PhD, gelly9@naver.com
Dong-Oh Kang, MD, PhD
- Not yet recruiting
Kyung Hee University Medical Center
Seoul
Jong-Shin Woo, MD, PhD, snowball77@hanmail.net
Jong-Shin Woo, MD, PhD
- Not yet recruiting
Seoul National University Boramae Medical Center
Seoul
Hyun Sung Joh, MD, PhD, wingx4@naver.com
Hyun Sung Joh, MD, PhD
- Not yet recruiting
Ajou University Hospital
Suwon
Hong-Seok Lim, MD,PhD, hslimmd@hanmail.net
Hong-Seok Lim, MD,PhD
- Not yet recruiting
Catholic University of Korea Uijeongbu St. Mary's Hospital
Uijeongbu-si
Chan Joon Kim, MD, PhD, godandsci@naver.com
Chan Joon Kim, MD, PhD
- Not yet recruiting
Wonju Severance Christian Hospital
Wŏnju
Jung-Hee Lee, MD, PhD, seranflute@gmail.com
Jung-Hee Lee, MD, PhD
About this study
Official title: Coronary Computed Tomography Angiography Versus Standard Care in High-Risk Patients After Percutaneous Coronary Intervention
The aim of the SMART-CARE trial is to compare clinical outcomes between coronary CT angiography (CCTA) versus standard care as follow-up strategies in high-risk patients after percutaneous coronary intervention (PCI).
Read the detailed description
Advancements in drug-eluting stents, physiology-guided treatment decisions, intravascular imaging-guided procedural optimization, and adjunctive medical therapy have significantly improved prognosis after percutaneous coronary intervention (PCI). However, high-risk patients-particularly those with complex coronary artery lesions or high-risk clinical conditions such as acute myocardial infarction with or without cardiogenic shock at presentation, diabetes mellitus which requires medical treatment (oral hypoglycemic agents or insulin), end-stage renal disease under dialysis, or multi-vascular disease-continue to have a significantly higher risk of adverse cardiovascular events. In this regard, meticulous follow-up, including periodic assessment of clinical and functional status, guideline-directed medical therapy (GDMT), and secondary prevention strategies are important, and current guidelines strongly recommend these measures as a Class I recommendation. However, recent randomized controlled trials have demonstrated that high-risk patients with complex coronary artery disease or high-risk clinical conditions still experience a continuous increase in adverse cardiovascular events despite optimal secondary prevention. This underscores the need for an optimized surveillance strategy to improve long-term prognosis.
Despite the emphasis on GDMT and secondary prevention in current guidelines, the most effective surveillance strategy after PCI remains uncertain. Existing recommendations primarily address secondary prevention and provide only limited guidance on surveillance for patients with previous coronary revascularization. Based on multiple randomized controlled trials, current guidelines do not recommend routine non-invasive stress testing or coronary CT angiography (CCTA) in asymptomatic patients receiving optimized GDMT (Class III, Level of Evidence B-R). However, this recommendation lacks direct evidence evaluating CCTA as a surveillance strategy after PCI. In patients with prior coronary revascularization, CCTA is currently recommended for assessing bypass graft or stent patency only in symptomatic patients (Class IIa), with limited supporting evidence (Level of Evidence B in ESC guidelines and Level of Evidence B-NR in ACC/AHA guidelines).
Notably, the SCOT-HEART trial demonstrated that a CCTA-based treatment strategy was superior to standard care, which relied on clinical and functional assessment along with as-needed non-invasive stress testing, in reducing a composite outcome of coronary heart disease death and non-fatal myocardial infarction. This suggests that a surveillance strategy incorporating CCTA may lead to improved subsequent management decisions, such as preemptive ischemia-driven revascularization or intensified medical therapy, potentially reducing ischemic cardiovascular events and mortality compared to standard guideline-recommended care.
To address this critical gap in clinical practice, we designed the Smart Angioplasty Research Team-Coronary CT Angiography versus Standard Care as Follow-up Strategies in High-Risk Patients after PCI (SMART-CARE) trial. This study aims to evaluate the impact of a CCTA-based surveillance strategy on clinical outcomes compared with standard guideline-directed follow-up in high-risk patients who have undergone PCI.
- Conditions
- Ischemic Heart Disease, Coronary Artery Disease
- Being tested
- Coronary CT Angiography (CCTA)
- Keywords
- coronary artery disease, percutaneous coronary intervention, coronary computed tomography angiography, follow-up strategy
- Medical subject headings
- Myocardial Ischemia, Coronary Artery Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Coronary CT Angiography (CCTA)Diagnostic test
In the surveillance by CCTA group, patients will be evaluated by CCTA at 1 year from index hospitalization. CCTA will be done according to current acquisition guidelines. Downstream management according to the results from CCTA will be performed under recommendations from current guidelines.
| Study group | Role | What they receive |
|---|---|---|
| Surveillance by CCTA Strategy Group | Experimental | In the surveillance by CCTA group, patients will be evaluated by CCTA at 1 year from index hospitalization. CCTA will be done according to current acquisition guidelines. Receives: Diagnostic Test: Coronary CT Angiography (CCTA) |
| Standard Care Strategy Group | No intervention | In the standard care group, patients will be managed according to the current guidelines. Regardless of symptoms, periodic visits will be performed by the charged physician. Secondary prevention including cardiovascular risk factor control, assessment of disease status, and comorbidities, and GDMT will be meticulously performed. In patients without a change in clinical or functional status, further evaluation by CCTA or non-invasive functional tests will not be performed. In this group, CCTA or non-invasive functional tests will be performed only for patients with significant change in clinical or functional status or with symptoms refractory to medical treatment.6,8 Whether patients will be referred for invasive coronary angiography will be determined by the charged physician according to patient's clinical or functional status and the results from CCTA or non-invasive functional tests according to current guidelines. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Time to first event of major adverse cardiac events (MACE)
MACE is a composite of death, non-fatal myocardial infarction (MI), hospitalization for acute coronary syndrome leading to an urgent revascularization, or stent thrombosis
Measured: 2 years after the last patient enrollment
Secondary outcomes (15)
All-cause death
All-cause death
Measured: 2 years after the last patient enrollment
Cardiac death
Cardiac death
Measured: 2 years after the last patient enrollment
Non-fatal MI
Non-fatal MI, defined by Forth Universal definition of MI
Measured: 2 years after the last patient enrollment
Spontaneous MI
Spontaneous MI, defined by Forth Universal definition of MI
Measured: 2 years after the last patient enrollment
Procedure-related MI (during follow-up period from invasive procedure)
Procedure-related MI (during follow-up period from invasive procedure), defined by Fourth Universal definition of MI
Measured: 2 years after the last patient enrollment
Hospitalization for acute coronary syndrome leading to an urgent revascularization
Hospitalization for acute coronary syndrome is defined as a clinical event in which the final diagnosis during unplanned hospitalization is acute coronary syndrome including spontaneous myocardial infarction or unstable angina.
Measured: 2 years after the last patient enrollment
Unplanned revascularization (clinically-driven)
All revascularization events will be adjudicated as either clinically-driven or non-clinically-driven. Revascularization will be considered clinically-driven if the diameter stenosis of the revascularized coronary segment is ≥50% by QCA and any of the following criteria for ischemia are met:
- A positive functional study corresponding to the area served by the target lesion; or
- Ischemic ECG changes at rest in a distribution consistent with the target vessel; or
- Typical ischemic symptoms referable to the target lesion; or ④ positive invasive physiologic test (fractional flow reserve ≤0.80 or instantaneous wave-free ratio ≤0.89); or ⑤ presence of stenosis with ≥70% diameter stenosis, even in the absence of other criteria Unplanned revascularization refers to revascularization not planned after initial assessments with invasive coronary angiography or non-invasive stress testing, depending on the allocated group, but performed due to clinical circumstances.
Measured: 2 years after the last patient enrollment
Definite stent thrombosis
Definite stent thrombosis, defined by Academic Research Consortium (ARC) II consensus
Measured: 2 years after the last patient enrollment
Rate of invasive coronary angiography during follow-up
Rate of invasive coronary angiography (with or without showing restenosis or obstructive CAD) during follow-up.
Angiographic restenosis was defined as a stenosis of at least 50 percent of the minimal luminal diameter in the target-lesion at invasive coronary angiography during follow-up. Obstructive or no obstructive coronary artery disease at invasive coronary angiography is defined as a visually estimated presence or absence of stenosis of 50% or more, as interpreted by the study-site staff, in any major epicardial vessel, including side branches of at least 2.5 mm in diameter.
Measured: 2 years after the last patient enrollment
Rate of revascularization by PCI or CABG during follow-up
Rate of revascularization by PCI or CABG during follow-up
Measured: 2 years after the last patient enrollment
Procedure-related complications from invasive procedure during follow-up
Procedure-related complications from invasive procedure during follow-up
Measured: 2 years after the last patient enrollment
Cerebrovascular accidents
Cerebrovascular accidents (ischemic or hemorrhagic)
Measured: 2 years after the last patient enrollment
Contrast-induced nephropathy or contrast-associated hypersensitivity reaction
Contrast-induced nephropathy, defined as an increase in serum creatinine of ≥0.5mg/dL or ≥25% from baseline within 48-72 hours after contrast agent exposure or contrast-associated hypersensitivity reaction
Measured: 2 years after the last patient enrollment
Total medical cost
Total medical cost
Measured: 2 years after the last patient enrollment
A composite of death or non-fatal MI
A composite of death or non-fatal MI
Measured: 2 years after the last patient enrollment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Jun 2025
- Study start2 Oct 2025
- Primary completion31 Dec 2031 (estimated)
- Study completion31 Dec 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Ischemic Heart DiseaseStudies of the same condition, open and under way.
- More trials run by Samsung Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Pragmatic, prospective, multi-center, open label, randomized controlled, superiority trial.
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 3,500 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Samsung Medical Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Joo Myung Lee, Samsung Medical Center
- Investigators
- Joo Myung Lee, MD, MPH, PhD, Principal investigator, Samsung Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07009418
- Sponsor's protocol ID
- SMC19801001
- Acronym
- SMART-CARE
- Status last verified
- Dec 2025
- First submitted
- 29 May 2025
- Last updated
- 19 Dec 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.
Study at a glance
From the registry record, last updated by the sponsor on 19 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Coronary Computed Tomography Angiography Versus Standard Care in High-Risk Patients After Percutaneous Coronary Intervention
- ClinicalTrials.gov ID
- NCT07009418
- Acronym / sponsor ID
- SMART-CARE / SMC19801001
- Conditions
- Ischemic Heart Disease, Coronary Artery Disease
- Keywords
- coronary artery disease, percutaneous coronary intervention, coronary computed tomography angiography, follow-up strategy
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 3,500 participants (estimated)
- Lead sponsor
- Samsung Medical CenterUniversity, hospital or other
- Study start
- 2 Oct 2025 (actual)
- Primary completion
- 31 Dec 2031 (estimated)
- Study completion
- 31 Dec 2032 (estimated)
- First posted
- 6 Jun 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the SMART-CARE trial is to compare clinical outcomes between coronary CT angiography (CCTA) versus standard care as follow-up strategies in high-risk patients after percutaneous coronary intervention (PCI).
Detailed description
Advancements in drug-eluting stents, physiology-guided treatment decisions, intravascular imaging-guided procedural optimization, and adjunctive medical therapy have significantly improved prognosis after percutaneous coronary intervention (PCI). However, high-risk patients-particularly those with complex coronary artery lesions or high-risk clinical conditions such as acute myocardial infarction with or without cardiogenic shock at presentation, diabetes mellitus which requires medical treatment (oral hypoglycemic agents or insulin), end-stage renal disease under dialysis, or multi-vascular disease-continue to have a significantly higher risk of adverse cardiovascular events. In this regard, meticulous follow-up, including periodic assessment of clinical and functional status, guideline-directed medical therapy (GDMT), and secondary prevention strategies are important, and current guidelines strongly recommend these measures as a Class I recommendation. However, recent randomized controlled trials have demonstrated that high-risk patients with complex coronary artery disease or high-risk clinical conditions still experience a continuous increase in adverse cardiovascular events despite optimal secondary prevention. This underscores the need for an optimized surveillance strategy to improve long-term prognosis.
Despite the emphasis on GDMT and secondary prevention in current guidelines, the most effective surveillance strategy after PCI remains uncertain. Existing recommendations primarily address secondary prevention and provide only limited guidance on surveillance for patients with previous coronary revascularization. Based on multiple randomized controlled trials, current guidelines do not recommend routine non-invasive stress testing or coronary CT angiography (CCTA) in asymptomatic patients receiving optimized GDMT (Class III, Level of Evidence B-R). However, this recommendation lacks direct evidence evaluating CCTA as a surveillance strategy after PCI. In patients with prior coronary revascularization, CCTA is currently recommended for assessing bypass graft or stent patency only in symptomatic patients (Class IIa), with limited supporting evidence (Level of Evidence B in ESC guidelines and Level of Evidence B-NR in ACC/AHA guidelines).
Notably, the SCOT-HEART trial demonstrated that a CCTA-based treatment strategy was superior to standard care, which relied on clinical and functional assessment along with as-needed non-invasive stress testing, in reducing a composite outcome of coronary heart disease death and non-fatal myocardial infarction. This suggests that a surveillance strategy incorporating CCTA may lead to improved subsequent management decisions, such as preemptive ischemia-driven revascularization or intensified medical therapy, potentially reducing ischemic cardiovascular events and mortality compared to standard guideline-recommended care.
To address this critical gap in clinical practice, we designed the Smart Angioplasty Research Team-Coronary CT Angiography versus Standard Care as Follow-up Strategies in High-Risk Patients after PCI (SMART-CARE) trial. This study aims to evaluate the impact of a CCTA-based surveillance strategy on clinical outcomes compared with standard guideline-directed follow-up in high-risk patients who have undergone PCI.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Pragmatic, prospective, multi-center, open label, randomized controlled, superiority trial.
| Arm | Type | Receives |
|---|---|---|
| Surveillance by CCTA Strategy Group | Experimental | Diagnostic Test: Coronary CT Angiography (CCTA)In the surveillance by CCTA group, patients will be evaluated by CCTA at 1 year from index hospitalization. CCTA will be done according to current acquisition guidelines. |
| Standard Care Strategy Group | No intervention | –In the standard care group, patients will be managed according to the current guidelines. Regardless of symptoms, periodic visits will be performed by the charged physician. Secondary prevention including cardiovascular risk factor control, assessment of disease status, and comorbidities, and GDMT will be meticulously performed. In patients without a change in clinical or functional status, further evaluation by CCTA or non-invasive functional tests will not be performed. In this group, CCTA or non-invasive functional tests will be performed only for patients with significant change in clinical or functional status or with symptoms refractory to medical treatment.6,8 Whether patients will be referred for invasive coronary angiography will be determined by the charged physician according to patient's clinical or functional status and the results from CCTA or non-invasive functional tests according to current guidelines. |
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- ① Patients aged 19 years old
- ② Patients who underwent successful PCI with one or more contemporary drug-eluting stents (stent diameter ≥3mm) or drug-coated balloons.
- ③ Patients must have at least one of the following criteria of complex coronary artery lesions or high-risk clinical characteristics:
- Complex coronary artery lesions:
- True bifurcation lesion (Medina 1,1,1/1,0,1/0,1,1) with side branch ≥2.5mm size ii. Chronic total occlusion (≥3 months) as target lesion iii. PCI for unprotected left main (LM) disease (LM ostium, body, distal LM bifurcation including non-true bifurcation) iv. Long coronary lesions (used stents or drug-coated balloons ≥38 mm in length) v. Multi-vessel PCI (≥2 major epicardial coronary arteries treated at one PCI session) vi. Multiple devices needed (≥3 more stents or drug-coated balloons per patient) vii. In-stent restenosis lesion as target lesion viii. Severely calcified lesion (encircling calcium in angiography) ix. Left anterior descending (LAD), left circumflex artery (LCX), and right coronary artery (RCA) ostial lesion
Key exclusion criteria (3 listed)
- ① Advanced chronic kidney disease (Creatinine clearance <30 ml/min/1.73 m2) not on dialysis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Coronary CT Angiography (CCTA)In the surveillance by CCTA group, patients will be evaluated by CCTA at 1 year from index hospitalization. CCTA will be done according to current acquisition guidelines. Downstream management according to the results from CCTA will be performed under recommendations from current guidelines. | Diagnostic test | Surveillance by CCTA Strategy Group |
Primary outcome
Time to first event of major adverse cardiac events (MACE)
Time frame: 2 years after the last patient enrollment
MACE is a composite of death, non-fatal myocardial infarction (MI), hospitalization for acute coronary syndrome leading to an urgent revascularization, or stent thrombosis
15 secondary outcomes
All-cause death
Time frame: 2 years after the last patient enrollment
Cardiac death
Time frame: 2 years after the last patient enrollment
Non-fatal MI
Time frame: 2 years after the last patient enrollment
Spontaneous MI
Time frame: 2 years after the last patient enrollment
Procedure-related MI (during follow-up period from invasive procedure)
Time frame: 2 years after the last patient enrollment
Hospitalization for acute coronary syndrome leading to an urgent revascularization
Time frame: 2 years after the last patient enrollment
Unplanned revascularization (clinically-driven)
Time frame: 2 years after the last patient enrollment
Definite stent thrombosis
Time frame: 2 years after the last patient enrollment
Rate of invasive coronary angiography during follow-up
Time frame: 2 years after the last patient enrollment
Rate of revascularization by PCI or CABG during follow-up
Time frame: 2 years after the last patient enrollment
Procedure-related complications from invasive procedure during follow-up
Time frame: 2 years after the last patient enrollment
Cerebrovascular accidents
Time frame: 2 years after the last patient enrollment
Contrast-induced nephropathy or contrast-associated hypersensitivity reaction
Time frame: 2 years after the last patient enrollment
Total medical cost
Time frame: 2 years after the last patient enrollment
A composite of death or non-fatal MI
Time frame: 2 years after the last patient enrollment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Dec 2025.
- Individual participant dataSharing planned: Yes. After publication of first manuscript and trial results, the de-identified data will be shared by permission of principle investigator, when asked.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Joo Myung Lee, MD, MPH, PhD principal investigator
Samsung Medical Center
22 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Coronary CT Angiography (CCTA) in people with Ischemic Heart Disease and Coronary Artery Disease, run by Samsung Medical Center at 22 sites 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 10 inclusion and 3 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 19 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 22 sites 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 Joo Myung Lee, MD, MPH, PhD (+82234102575, drone80@hanmail.net), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Time to first event of major adverse cardiac events (MACE) (time frame: 2 years after the 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 19 Dec 2025.