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Impact of Colchicine on Coronary Flow, Plaque Vulnerability, and Thrombogenicity in Acute Myocardial Infarction (AMI) with Multi-vessel Disease (MVD): Randomized, Double-Blinded, Controlled Pilot Trial

Impact of Colchicine on Coronary Flow, Plaque Vulnerability, and Thrombogenicity in Acute Myocardial Infarction (AMI) with Multi-vessel Disease (MVD): Randomized, Double-Blinded, Controlled Pilot Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011025
Enrollment
72
Registered
2025-09-12
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

None listed

Interventions

Drug : Pre-Procedure Medication: All patients will receive a loading dose of 300 mg of aspirin and 180 mg of ticagrelor prior to undergoing percutaneous coronary intervention (PCI). Anticoagulation:

Sponsors

Gyeongsang National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Subject must be =18 years 2) Patients with a diagnosis of AMI by symptom, cardiac marker and electrocardiographic change of ST-elevation myocardial infarction or Non ST elevation myocardial infarction. 3) Thrombolysis in Myocardial Infarction flow 0, 1, or 2 before the procedure; 4) Achievement of Thrombolysis In Myocardial Infarction 3 flow after balloon angioplasty or thrombus aspiration 5) Subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of receiving invasive physiologic or imaging evaluation and he/she or his/her legally authorized representative provides written informed consent to any study related procedure.

Exclusion criteria

Exclusion criteria: 1) Cardiogenic shock (systolic blood pressure 90mmHg) or cardiac arrest 2) Rescue percutaneous coronary intervention after fibrinolysis 3) Acute occlusion of left main coronary artery 4) Major coronary dissection (type D–F) after procedures achieving Thrombolysis In Myocardial Infarction 3 flow 5) ST elevation myocardial infarction caused by stent thrombosis, 6) Non-cardiac co-morbid conditions are present with life expectancy <2 year (per site investigator’s medical judgment). 7) Inability to undergo invasive coronary physiologic assessment 8) Inability to undergo anatomical assessment (Optical Coherence Tomography, OCT) 9) Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Comparison of changes in coronary flow reserve (CFR) and index of microcirculatory resistance (IMR) in non-infarct related artery (non-IRA) between the two groups

Secondary

MeasureTime frame
Comparison of changes in thin-cap fibroatheroma (TCFA) and plaque in non-infarct related artery (non-IRA) between the two groups;Comparison of changes in thromboelastography (TEG) and fibrinogen between the two groups;Comparison of changes in high-sensitivity C-reactive protein (hs-CRP), fibrinogen, and D-dimer between the two groups

Countries

Korea, Republic of

Contacts

Public ContactYunjeong Song

Gyeongsang National University Hospital

dbswjddbswjd87@naver.com+82-55-750-9078

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026