Phase 3 Stroke Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged between 18 and 80 years old
- People who have been diagnosed with a spontaneous brain bleed (not caused by injury or another known condition) in the upper part of the brain, confirmed by a brain scan
- People who arrived at hospital within 24 hours of their symptoms starting (or within 24 hours of when they were last seen to be well)
- People whose brain bleed covers an area of at least 10 mL on the scan, or any size if surgery has already been performed
- People with a stroke severity score above 8 on a standard medical scale called the NIHSS (confirm with trial site)
- People with a level of consciousness score of 8 or higher on a scale called the Glasgow Coma Scale (confirm with trial site)
- People for whom written consent has been provided — either by the patient themselves or by an approved person acting on their behalf
Who may not be able to join:
- People whose brain bleed was caused by a known underlying condition, such as an abnormal blood vessel, a brain aneurysm, a tumour, or a head injury — or where the bleed is a result of a stroke caused by a blockage
- People whose bleeding is only inside the fluid-filled spaces of the brain (isolated intraventricular haemorrhage)
- People with chronic kidney disease
- People considered very likely to pass away within 7 days, or who are unlikely to be able to follow the study treatment and check-up schedule
- People with serious ongoing health conditions that could affect how outcomes are measured, such as cancer, chronic lung disease, heart failure, or significant existing disability
- People who are pregnant or breastfeeding
- People who have previously had chelation therapy, or who have a known allergy or sensitivity to deferoxamine (one of the study drugs)
- People with severely low iron levels in the blood (haemoglobin below 7 g/dL or needing regular blood transfusions)
- People currently taking iron supplements containing more than 325 mg of ferrous iron
- People with a blood creatinine level above 2 mg/dL, which indicates reduced kidney function (confirm with trial site)
- People with known heart failure who are also taking more than 500 mg of vitamin C
- People who are allergic to colchicine (another study drug)
- People with certain bone marrow or severe liver or kidney conditions (confirm with trial site)
- People taking certain medications that are known to interact with colchicine, such as some antifungal medicines like ketoconazole or fluconazole (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 4039448107
Australian sites
4039448107
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
mRS scores at 6 months analysed with utility-weights
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.