Anti-inflammatory Effects of Colchicine in PCI

NYU Langone Health

Status and phase: Completed; Phase 4

Conditions: Coronary Artery Disease

Treatments: Drug: Placebo; Drug: Colchicine

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01709981

11-02573

Details and patient eligibility

About

Peri-procedural inflammation is associated with increased rates of post-procedural myocardial infarction (MI), which occur in up to 35% of PCI patients and are themselves associated with increased risk of later MI and death. Statins suppress both inflammatory markers and MI rates during and after PCI, but ≥ 40% of PCI patients go statin-untreated, due in part to side effects such as myalgia. Moreover, because their mechanism of action relies on post-translational effects, statins must be given ≥ 12 to 24 hours prior to PCI, a time frame that is not always feasible. The investigators propose a novel alternative approach to reduce inflammation during PCI employing colchicine, an anti-inflammatory medication used frequently in gout and pericarditis. Colchicine may be particularly applicable to the PCI setting due to its rapid onset of action and excellent side-effect profile at low doses, as well as its known mechanisms of action. However, data on colchicine use in patients with coronary disease is extremely limited, and no studies to date have evaluated the use of colchicine in patients undergoing PCI. The investigators aim to characterize a potential mechanism of benefit in patients undergoing PCI by evaluating the effects of colchicine on soluble and leukocyte surface markers after PCI. The investigators also aim to determine the effects of colchicine on peri-procedural myonecrosis and MI. Accordingly, the investigators propose a prospective randomized study to characterize the effect of colchicine on inflammation and peri-procedural myocnecrosis. Patients referred for possible PCI will be randomized in a double-blinded fashion to placebo or colchicine (1.2mg 1 to 2 hours before PCI, followed by 0.6mg 1 hour later). The primary endpoint will be post-procedural interleukin-6 level. Secondary endpoints will include other relevant soluble and leukocyte-associated inflammatory markers. Sample size needed is 200 patients undergoing PCI. To adjust for a floor effect, 280 patients undergoing PCI will be needed. 400 patients will likely be needed to be enrolled to reach 280 PCIs (the remaining will have undergone a diagnostic only procedure). Of note, this is a substudy of the COLCHICINE-PCI trial (NCT 02594111)

Enrollment: 280 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients must be more than 18 years of age and referred for coronary angiography

Exclusion criteria

• Plan for diagnostic-only coronary angiography
• On colchicine chronically
• History of intolerance to colchicine
• Glomerular filtration rate <30mL/minute or on dialysis
• Active malignancy or infection
• History of myelodysplasia
• High-dose statin load <24 hours prior to procedure
• Use of oral steroids or non-steroidal anti-inflammatory agents other than aspirin within 72 hours or 3 times the agent's half-life (whichever is longer)
• Use of strong CYP3A4/P-glycoprotein inhibitors (specifically ritonavir, ketoconazole, clarithromycin, cyclosporine, diltiazem and verapamil)
• Unable to consent
• Participating in a competing study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Quadruple Blind

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280 participants in 2 patient groups, including a placebo group

Colchicine

Experimental group

Description:

1.2mg colchicine 1 to 2 hours prior PCI, followed by 0.6mg one hour later

Treatment:

Drug: Colchicine

Placebo

Placebo Comparator group

Description:

Placebo 1-2 hours prior PCI, followed by placebo 1 hour later

Treatment:

Drug: Placebo