Phase 3 Stroke Trial, Recruiting NCT06763055 Sponsor: The George Institute Condition: Stroke
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Phase 3 Stroke Trial, Recruiting

NCT06763055
Recruiting Phase 3 🇦🇺 Australian site

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 19 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 4039448107

Australian sites

Royal Prince Alfred Hospital, Sydney, New South Wales
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

Status
Recruiting
Phase
Phase 3
Sponsor
The George Institute
Registry
ClinicalTrials.gov
Start date
27 February 2025
Est. completion
1 January 2028

Where this trial is recruiting

🇦🇺 Australia 🇨🇳 China

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov