Brain Cancer Trial, Recruiting NCT06560372 Sponsor: University Hospital Center of Martinique Condition: Brain Cancer
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Brain Cancer Trial, Recruiting

NCT06560372
Recruiting Not Applicable

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:

  • Adults aged 18 or older
  • People who are hospitalised at the Martinique University Hospital for treatment or monitoring of a moderate or severe traumatic brain injury (a serious head injury, measured by a standard medical score of 13 or below at the time of first treatment)
  • People whose brain scan shows a specific type of bleeding around the brain (called subarachnoid haemorrhage)
  • People who have given free, written, and informed consent — or, if they are unable to do so, whose legal representative has given consent on their behalf
  • People included under an emergency consent procedure (where a representative could not initially be reached), provided the representative or patient is informed and gives written agreement within the first 48 hours
  • People who are enrolled in a social security (health insurance) scheme

Who may not be able to join:

  • People who are pregnant
  • People who have a known or newly diagnosed aneurysm (a bulge in a blood vessel in the brain)
  • People with a known history of severe chronic kidney disease (stage 4, meaning kidney function is significantly reduced — confirm with trial site)
  • People for whom death is considered imminent
  • People who meet criteria that would prevent admission to critical care — for example, death is expected within 48 hours, a serious life-limiting illness is expected to cause death within 30 days, or the person is receiving palliative (end-of-life comfort) care
  • People with a known allergy to iodine-based contrast dye (a substance used in certain medical scans)
  • People who are under a legal protection order, guardianship, or curatorship
  • People whose representative (or the person themselves) has declined participation in the study
  • People whose death becomes expected within the first 48 hours after joining the trial
  • People who are under 18 years of age
  • People who leave the hospital against medical advice
  • People who are transferred to a different hospital before day 13 of treatment
  • People whose representative (or the person themselves, after recovery) withdraws consent to participate, including withdrawal of permission to use already-collected data

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 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Marie SABIA, PhD, University Hospital Center of Martinique

Phone: 05 96 55 10 54

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
Not Applicable
Sponsor
University Hospital Center of Martinique
Registry
ClinicalTrials.gov
Start date
6 November 2024
Est. completion
6 November 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Estimate the incidence of cerebral vasospasm (CV) with clinical impact in moderate to severeTBI patients complicated by subarachnoid hemorrhage (SAH) at Martinique University Hospital.

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: 26 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