Colchicine Treatment for Non-Flow-Limiting Coronary Plaque by Coronary CTA: A Randomized Controlled Trial

Overview

This study is a prospective, multicenter, randomized controlled clinical trial designed to evaluate whether an anti-inflammatory medication can help improve heart health in patients with stable coronary artery disease. 1. Research Question \& Hypothesis We aim to determine whether adding low-dose colchicine (0.5 mg once daily) to standard medical treatment can further reduce the risk of major cardiovascular events in patients with chronic coronary syndromes (CCS), especially those with non-flow-limiting coronary plaques detected by coronary CT angiography (CCTA). We hypothesize that colchicine, by reducing vascular inflammation, may help prevent future heart attacks, strokes, and the need for coronary revascularization. 2. Study Population \& Design Design: A rigorously designed, prospective, multicenter, randomized (1:1), controlled superiority trial. Population: Adults (\>18 years) diagnosed with CCS, identified by CCTA as having at least one coronary artery with ≥50% narrowing but without significant impact on blood flow (CT-FFR \> 0.80). Intervention: Intervention Group: Standard guideline-directed medical therapy (GDMT) + colchicine 0.5 mg once daily Control Group: GDMT alone Sample Size: Approximately 3,826 participants, accounting for a 5% dropout rate. 3. Study Endpoints Primary Endpoint: The occurrence of major adverse cardiovascular or cerebrovascular events (MACCE), including:Cardiovascular death; Ischemic stroke; Non-fatal myocardial infarction; Any coronary revascularization. Assessed for 12 months after the last patient is enrolled. Secondary Endpoints:Occurrence of MACCE over 36 months. Incidence and time to first occurrence of each event category at 12, 24, and 36 months. Safety Endpoint: Side effects related to colchicine (e.g., gastrointestinal upset, liver or kidney abnormalities, blood disorders, muscle-related reactions).

Interventions

• Drug Colchicine combined with Guideline-Directed Medical Therapy
  colchicine combined with guideline-directed medical therapy group

Primary outcome measures

• Major adverse cardiovascular and cerebrovascular events (MACCE) [Time frame: 12 months after enrollment]

Eligibility criteria

Inclusion criteria

• The subject (or legal guardian) understands the trial requirements and treatment procedure, and signs the written informed consent before undergoing any protocol-specified examinations or procedures;
• Aged ≥18 years;
• Clinically diagnosed with chronic coronary syndrome (CCS);
• CCTA confirms ≥50% stenosis in at least one epicardial coronary artery, and CT fractional flow reserve (CT-FFR) >0.80.

Exclusion criteria

• Unable or unwilling to provide informed consent;
• Unable to complete scheduled follow-up;
• Underwent PCI within the past 3 months;
• History of coronary artery bypass grafting (CABG);
• Diagnosis of acute coronary syndromes (ACS);
• No coronary plaque or plaque stenosis <50% (confirmed by CCTA);
• Lesion-specific CT-FFR ≤0.80 in at least one major epicardial coronary artery;
• Inflammatory bowel disease (Crohn's disease/ulcerative colitis) or chronic diarrhea;
• History of gastric ulcer or gastric bleeding;
• Pregnant/lactating women or women of childbearing age without effective contraception;
• Neuromuscular disease or non-transient creatine kinase (CK) >3×upper limit of normal (ULN) (confirmed by ≥2 lab tests);
• Clinically significant non-transient hematological abnormalities (hemoglobin <100 g/L, hematocrit <30%/ >52%, white blood cell count <3×10⁹/L, platelet count <100×10⁹/L; confirmed by ≥2 lab tests);
• Estimated glomerular filtration rate (eGFR) <30 mL/min/1.73 m² (CKD-EPI formula);
• Liver dysfunction (alanine aminotransferase >3×ULN and/or total bilirubin >2×ULN);
• Current/planned immunosuppressive therapy;
• Long-term colchicine use for other indications;
• Definite/suspected colchicine allergy;
• Active malignant tumor (expected survival <1 year);
• Use of potent CYP3A4/P-glycoprotein inhibitors (e.g., cyclosporine, antiretrovirals, antifungals, erythromycin, clarithromycin) without alternative drugs.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Single blind

Primary purpose

Treatment

Study locations

China · 1 center

• Nanjing First Hospital — Nanjing

Identifiers

NCT: NCT07349875 · KY20241217-10-KS-02

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗