Assessment of Inflammatory mediator release, microvascular resistance, and plaque morphology after percutaneous coronary intervention in patients treated with colchicine.
- Conditions
- coronary artery diseaseacute coronary syndromestable coronary artery diseaseCardiovascular - Coronary heart disease
- Registration Number
- ACTRN12619001449123
- Lead Sponsor
- The Heart Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria: Patients (>21yrs) with a clinical need for cardiac catheterisation at Royal
Prince Alfred Hospital will be invited to participate in the study.
Patients with greater than 50% stenosis in the left main coronary artery, cardiogenic shock or haemodynamic instability will be excluded from the study. Other exclusion criteria include age <21, pregnancy, those unable to make their own decisions, patients with moderate renal dysfunction (creatinine clearance <50 ml/min) or hepatic dysfunction (ALT [1.5 x upper limit of normal range); thrombocytopenia or leukopenia; pregnant or lactating women and women at risk of pregnancy. Patients already taking colchicine, those with evidence of active infection or inflammatory conditions that might be associated with markedly elevated hs-CRP levels in the blood (e.g., active rheumatoid arthritis) and those taking other anti-inflammatory therapies (e.g. corticosteroids) or strong CYP3A4 inhibitors will also be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method