Colchicine for the Stability of Coronary Plaque in Acute Coronary Syndrome (COLOCT)

Acute Coronary Syndrome Clinical Trial

— COLOCT  

Official title:

The Efficacy and Safety of Colchicine in Improving the Stability of Coronary Plaque in Patients With Acute Coronary Syndrome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04848857
• Other study ID #: CTACS202001
• Status: Completed
• Phase: Phase 4
• Start date: May 3, 2021
• Est. completion date: October 5, 2023

Study information

• Verified date: December 2023
• Source: Wuhan Union Hospital, China
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Evidence from the COLCOT Trial has shown that anti-inflammatory effect of colchicine reduced the risk of cardiovascular events in patients with recent myocardial infarction. We hypothesized that this might be due to the improvement of the coronary plaque stability by colchicine. Optical coherence tomography (OCT) is the most precise method to detect plaque stability in clinical practice. Thus, the purpose of this study is to evaluate the efficacy and safety of colchicine on improving the stability of coronary plaque in patients with acute coronary syndrome.

Description:

This is a single-center, randomized, double-blind, placebo-controlled clinical trial. OCT coronary images analyzed at an independent imaging core laboratory (Department of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, China) by blinded expert readers.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 128
• Est. completion date: October 5, 2023
• Est. primary completion date: August 20, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Participants who understand and sign the informed consent form voluntarily.

2. Age = 18 years old and = 80 years old, regardless of sex.

3. hospitalized patients diagnosed with acute coronary syndrome within 1 month.

4. at least one non-culprit lesion with diameter stenosis percentage of 30% to 70% by visual estimation on coronary angiography (CAG) after completing any planned percutaneous revascularization.

5. the lesion shown by OCT was lipid-rich plaque (Lipid pool arc > 90 °).

Exclusion Criteria:

1. Allergic to colchicine.

2. Colchicine was taken within 10 days before randomization.

3. Abnormal liver function (ALT > 3 times the upper limit of normal value).

4. Abnormal renal function (creatinine clearance rate < 45 ml/min).

5. Thrombocytopenia (PLT < 100G/L).

6. Uncontrolled infectious diseases during the screening period.

7. Known immune diseases or immune-related diseases such as systemic lupus erythematosus, asthma, inflammatory bowel disease, gout, malignant tumor and so on.

8. Pre-existing or plan for the administration of systemic anti-inflammatory treatments such as non-steroidal anti-inflammatory drugs, hormones, immunomodulatory and chemotherapeutic drugs.

9. History of surgery or interventional therapy within 6 months prior to the screening period.

10. A history of coronary artery bypass grafting or a plan for coronary artery bypass grafting within 1 year.

11. Left main coronary disease (=50% reduction in lumen diameter by angiographic visual estimation).

12. Significant coronary calcification or tortuosity deemed to preclude OCT evaluation.

13. Diagnosed with mental disorders such as anxiety or depression.

14. Pregnant women, lactating women or women of childbearing age who do not use effective contraceptive methods.

15. Participated in other clinical trials within 3 months before the screening period.

16. Do not receive standardized treatment after being diagnosed with coronary heart disease.

17. The life expectancy of the subjects is less than 1 year.

18. The researchers determined that other conditions in which the patient was not suitable to participate in the clinical trial.

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Syndrome

Intervention

Drug:
• Colchicine
colchicine is a potent anti-inflammatory drug which is currently recommended for the treatment of pericarditis and acute gout attacks, but also familial Mediterranean fever and Behçet disease. This drug acts on inflammation through inhibition of microtubule polymerization by binding free tubule dimers. Colchicine blunts monocyte and neutrophil invasion at the site of inflammation and reduces intracellular trafficking and thus the release of cytokine and production of reactive oxygen species and a variety of proteolytic enzymes.
• Placebo
the placebo is a drug with no chemical effects but with the same physical characteristics as the experiment drug colchine.

Locations

Country	Name	City	State
China	Wuhan Union Hospital	Wuhan	Hubei

Sponsors (1)

Lead Sponsor	Collaborator
Wuhan Union Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	changes of the Thickness of fibrous cap of coronary artery plaque	changes of the thickness of fibrous cap of coronary artery plaque measured by OCT	12 months
Secondary	changes of the Average lipid arc of coronary artery plaque	changes of the average lipid arc of coronary artery plaque measured by OCT	12 months
Secondary	changes of the Macrophage accumulation in coronary artery plaque	changes of the macrophage accumulation in coronary artery plaque measured by OCT	12 months
Secondary	changes of the Incidence of thin-cap fibroatheroma (TCFA)	changes of the incidence of TCFA measured by OCT	12 months
Secondary	changes of the Minimum lumen area (MLA)	changes of the MLA measured by OCT	12 months
Secondary	changes of the inflammatory biomarkers (hsCRP, IL-6, and MPO)	changes of the inflammatory biomarkers (hsCRP, IL-6, and MPO)	12 months
Secondary	major adverse cardiovascular and cerebrovascular events (MACCEs)	A composite of all-cause death, nonfatal myocardial infarction, nonfatal stroke, revascularization due to ischemia	12 months