Colchicine for the Reduction of Dependency and Vascular Events After an Acute Intracerebral Hemorrhage
NCT ID: NCT06587737
Last Updated: 2025-01-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE3
1125 participants
INTERVENTIONAL
2025-06-30
2028-06-30
Brief Summary
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The objective of CoVasc-ICH 2 is to demonstrate that oral colchicine 0.5 mg daily is superior to placebo for improving the outcomes of ICH survivors with evidence or risk factors for atherosclerosis, when started within 72 hours from ICH onset.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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colchicine 0.5mg OD
Colchicine 0.5 MG
colchicine 0.5mg once-daily
placebo
Placebo
matching placebo, lacking active ingredient, once-daily
Interventions
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Colchicine 0.5 MG
colchicine 0.5mg once-daily
Placebo
matching placebo, lacking active ingredient, once-daily
Eligibility Criteria
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Inclusion Criteria
i. history of symptomatic coronary, peripheral and/or carotid artery disease (severe atherosclerotic vascular disease), or ii. visualized extracranial cervical/intracranial atherosclerotic disease causing any degree of stenosis/occlusion or presence of aortic arch plaque with maximum thickness ≥1 mm (moderate atherosclerotic vascular disease), or iii. two or more risk factors including: age 60 years or older, hypertension, dyslipidemia, diabetes mellitus, chronic kidney disease (eGFR: 15-50mL/min), history of ischemic stroke or current smoking (mild atherosclerotic vascular disease).
Exclusion Criteria
* ICH volume more than 60ml in the last imaging scan prior to consent
* Glasgow Coma Scale (GCS) score less than 7 or being intubated at the time of consent
* inflammatory bowel disease or chronic diarrhea
* cirrhosis or severe hepatic dysfunction
* renal insufficiency (eGFR\<15mL/min)
* concurrent or planned treatment with strong CYP3A4 inhibitors (atazanavir, clarithromycin, darunavir/ritonavir, indinavir, itraconazole, ketoconazole, lopinavir/ritonavir, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, tipranavir/ritonavir) or P-gp inhibitors (cyclosporine, ranolazine)
* pregnancy or breast-feeding
* known allergy or sensitivity to colchicine
* a strong indication for colchicine where assignment to placebo is deemed unacceptable
* estimated life expectancy less than 6 months at the time of enrollment, and
* inability to adhere to study procedures
18 Years
ALL
No
Sponsors
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Population Health Research Institute
OTHER
Responsible Party
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Principal Investigators
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Aristeidis Katsanos, MD
Role: PRINCIPAL_INVESTIGATOR
Population Health Research Institute, Hamilton Health Sciences, McMaster University
Ashkan Shoamanesh, MD
Role: PRINCIPAL_INVESTIGATOR
Population Health Research Institute, Hamilton Health Sciences, McMaster University
Central Contacts
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Other Identifiers
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CoVasc-ICH 2
Identifier Type: -
Identifier Source: org_study_id
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