Brain Cancer Trial, Recruiting NCT05977803 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Brain Cancer
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Brain Cancer Trial, Recruiting

NCT05977803
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 over 18 years
  • People who have been diagnosed with primary lung cancer confirmed by a tissue sample (biopsy)
  • People who have brain metastases (cancer that has spread to the brain), whether confirmed by tissue sample or not
  • People whose brain metastases have been treated with radiation therapy
  • People who are enrolled in a treatment plan for brain metastases using whole-brain radiation, stereotactic radiation, or gamma-knife radiation
  • People whose follow-up MRI scan has shown that one or more brain metastases lesions have grown or changed in size
  • People who are enrolled in a social security (health insurance) scheme

Who may not be able to join:

  • People who have indicated they do not wish to take part in the study
  • People for whom MRI scans are not medically safe (for example, due to certain implants or devices)
  • People who have declined to have imaging performed
  • People receiving state medical aid, unless a specific exemption applies (confirm with trial site)
  • People with severe cognitive difficulties that would prevent them from giving informed consent
  • People who are under legal guardianship or who are currently detained

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 20 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: Augustin Gaudemer, MD, Assistance Publique - Hôpitaux de Paris

Phone: 01 40 25 76 13

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
Registry
ClinicalTrials.gov
Start date
15 February 2024
Est. completion
15 February 2029

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Visually significant hyperperfusion on normalized cerebral blood flow mapping generated from T2* infusion data with injection, confirmed by quantitative measurement of a ratio > 2.5 between tumor DSC and contralateral white matter.

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: 20 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