Efficacy and Safety of Colchicine After PCI

After informed consent, 8862 subjects who meet all inclusion will be randomly assigned to receive colchicine (0.5 mg/day), colchicine (0.375 mg/day), or placebo (1:1:1 allocation ratio), with follow-up at months (1, 6, 12, 18, 24…) after randomization, and phone assessments at months (3, 9, 15, 21…). The occurrence of any endpoints or other adverse events will be assessed every 3 months. Subjects will also receive standard medical care for antiplatelets, control of dyslipidemia, hypertension, angina and diabetes as directed by national guidelines. All suspected cardiovascular endpoints will be adjudicated by the Clinical Event Committee (CEC, consisting of three experienced members blinded as to allocation of therapy). The Data and Safety Monitoring Board (DSMB, consisting of five fully independent members) will review unblinded safety data as detailed in the DSMB charter. An interim analysis is planned after approximately 50% of primary endpoints have been positively adjudicated. The DSMB charter will pre-specify the methodology for the interim analysis and the rules for early termination of the study.

Inclusion criteria

• (1) Capable and willing to provide informed consent;
• (2) Age ≥18 and ≤80 years old, regardless of sex;
• (3) Hospitalized patients with CHD requiring PCI;
• (4) Completion of all planned PCI during hospitalization;
• (5) Standardized treatment of coronary artery disease according to national guidelines.

Exclusion criteria

• (1) Known allergy to colchicine;
• (2) Colchicine taken within 10 days prior to randomization group;
• (3) Patients currently in cardiogenic shock or hemodynamically unstable;
• (4) Patients with known inflammatory bowel disease or chronic diarrhea;
• (5) Abnormal liver function (ALT> 3 times the upper limit of normal);
• (6) Abnormal renal function (eGFR<30mL/min/1.73m2);
• (7) Active malignant tumors reported in past medical history;
• (8) Existing or planned treatment with other anti-inflammatory or immunosuppressive drugs;
• (9) Pregnant women, lactating women or women of childbearing age who did not use effective contraceptives;
• (10) Any other circumstances in which the investigator judges that the patient is not suitable to participate in the clinical trial.