Colchicine for the Reduction of Dependency and Vascular Events After an Acute Intracerebral Hemorrhage

NCT ID: NCT06587737

Last Updated: 2025-01-15

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

1125 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-30

Study Completion Date

2028-06-30

Brief Summary

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Data indicate that patients with intracerebral hemorrhage (ICH) are at high risk for thromboembolic events and disability that is not being sufficiently mitigated by current treatment strategies. This is aggravated by the cessation of antithrombotic medications for significant periods after hemorrhage. These findings highlight the need for novel treatments that modify the high risk for major vascular events and functional outcomes in ICH survivors.

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.

Detailed Description

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Conditions

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Colchicine ICH - Intracerebral Hemorrhage Stroke Dependence

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Double-blind, randomized, placebo-controlled, phase III study
Primary Study Purpose

PREVENTION

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors
Double-blind

Study Groups

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colchicine 0.5mg OD

Group Type EXPERIMENTAL

Colchicine 0.5 MG

Intervention Type DRUG

colchicine 0.5mg once-daily

placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

matching placebo, lacking active ingredient, once-daily

Interventions

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Colchicine 0.5 MG

colchicine 0.5mg once-daily

Intervention Type DRUG

Placebo

matching placebo, lacking active ingredient, once-daily

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Adult patients presenting with spontaneous intraparenchymal hemorrhage within 72 hours of symptom onset and qualifying for at least one of the following categories:

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

* secondary causes of ICH (such as trauma, macrovascular anomalies, neoplasms or bleeding diathesis)
* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Population Health Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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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Kevin W Reeh, MSc

Role: CONTACT

905-521-2100

Amanda Taylor, BSc

Role: CONTACT

Other Identifiers

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CoVasc-ICH 2

Identifier Type: -

Identifier Source: org_study_id

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