Heart Failure
Conditions
Brief summary
The goal of this 2x2 factorial clinical trial is to test the efficacy of i) colchicine, and ii) thiamine in heart failure (HF) secondary to ischemic heart disease. The main questions it aims to answer are: * Does colchicine reduce the risk of cardiovascular (CV) death, a HF event, or an ischemic CV event * Does thiamine reduce the risk of cardiovascular (CV) death, or a HF event Participants will undergo the following procedures: * Run-in: All participants will receive colchicine 0.5 mg daily to assess drug tolerance over a 3-4 week period. * Randomization: If colchicine is tolerated during run-in, eligible participants will be randomized in a 2x2 factorial design to receive i) colchicine 0.5mg daily or placebo, and ii) thiamine 300mg daily or no thiamine. * Follow-up: Clinical outcomes, side effects, adverse events, and drug adherence will be captured during follow-up
Interventions
DRUGColchicine 0.5 MG
Oral colchicine 0.5 mg daily
Placebo colchicine daily
DRUGThiamine Mononitrate 300 mg
Thiamine Mononitrate 300 mg daily
Sponsors
Population Health Research Institute
Canadian Institutes of Health Research (CIHR)
Hamilton Health Sciences Corporation
Study design
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Masking description
Factorial 1: Placebo controlled. Factorial 2: Prospective Randomized Open Blinded End-point (PROBE) design
Intervention model description
Factorial 1: Colchicine 0.5 mg daily or placebo Factorial 2: Thiamine 300mg daily or no thiamine
Eligibility
Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age \>/= 45 years 2. Documented ischemic HF as the etiology of HF, which includes: 1. a prior history of CAD (defined as a history of myocardial infarction, coronary artery bypass graft surgery, percutaneous coronary intervention, or non-invasive or invasive cardiac testing consistent with a diagnosis of CAD), and 2. determination of CAD to be the cause primary cause of HF based on local investigator assessment 3. New York Heart Association (NYHA) class II-IV symptoms 4. Documented LVEF \</= 45% within 1 year prior to enrollment 5. Optimization of HF treatment based on local practice. 6. Ambulatory HF patients or stable hospitalized patients with HF will both be eligible for enrollment in the trial. For hospitalized patients, enrollment will require i) evidence of clinical stability from HF defined as no use of an inotropic agent or intravenous diuretic agent in the prior 24, and ii) expected discharge from hospital in the next 72 hours.
Exclusion criteria
1. Female who is pregnant, breast-feeding, or of childbearing potential and not using an effective form of birth control\* 2. Regular or required use colchicine or thiamine for other clinical indications.\*\* 3. History of allergic reaction to colchicine or to thiamine; or current or planned use of cyclosporine, verapamil, diltiazem, azole antifungal, macrolide antibiotic (except azithromycin), or HIV protease inhibitor 4. Use of a ventricular assist device or prior heart transplant 5. Coronary revascularization (coronary artery bypass graft surgery or percutaneous coronary intervention) within the 4 weeks prior to enrollment, or planned within the next 4 weeks. 6. Severe valvular disease 7. Chronic and severe renal dysfunction defined as eGFR \< 15 mL/min/1.73m2 based on local laboratory measurement done within 6 months prior to run-in\*\*\* 8. History of liver cirrhosis 9. Active malignancy (excluding basal cell or treated squamous cell carcinoma of the skin) requiring treatment and with a life-expectancy of \< 2 years. 10. Concurrent use of other experimental pharmacologic agents -
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Colchicine arm: Time to first occurrence of a CV death, a HF event, MI, stroke, or arterial revascularization | 3.5 years |
| Thiamine arm: Time to first occurrence of a CV death, or a HF event | 3.5 years |
Secondary
| Measure | Time frame |
|---|---|
| Time to death | 3.5 years |
| Time to first hospitalization | 3.5 years |
Countries
Canada
Contacts
Primary ContactPhilip G Joseph, M.D.
Outcome results
None listed