Brain Cancer Trial, Recruiting NCT05124236 Sponsor: Susanne Rogers Condition: Brain Cancer
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Brain Cancer Trial, Recruiting

NCT05124236
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:

  • People aged 18 or older
  • People who have signed and dated a consent form and are willing to follow all study procedures for the full duration of the trial
  • People whose general health and ability to carry out daily activities meets a minimum level, as measured by a standard medical scoring scale called the Karnofsky scale (score of 60 or above)
  • People who have a confirmed cancer diagnosis (either a primary tumour or one that has spread from elsewhere in the body), based on tissue testing
  • People who are able to take steroid medications
  • People who are able to have an MRI scan (no medical reasons preventing this)
  • People whose MRI scan shows a clearly defined, contrast-enhancing brain metastasis no larger than 4.0 cm that a specialist tumour board has recommended for surgical removal, and who have no more than 3 other brain metastases that could be treated with a focused type of radiation therapy
  • People whose treating doctor estimates they have a life expectancy of more than 12 months
  • People whose blood test results meet minimum levels for platelets, clotting function, and haemoglobin (confirm specific values with trial site)

Who may not be able to join:

  • People whose cancer is of a type known as radiosensitive — specifically germ cell tumour, lymphoma, or multiple myeloma
  • People showing signs of significant pressure building inside the skull that would require urgent surgery (such as a midline shift greater than 10 mm or compression of certain brain structures)
  • People with more than 4 brain metastases in total, or whose metastasis being considered for removal is larger than 4.0 cm
  • People who have more than one brain metastasis that would require surgical removal
  • People with cancer that has spread to the lining or fluid surrounding the brain or spinal cord (unless it is in a limited area that can be treated with radiation at the same time as the surgery)
  • People who have previously received radiation treatment to the brain, including focused radiation to the specific lesion being considered or whole-brain radiation
  • People who have previously had surgery to remove a brain tumour (whether primary or secondary)
  • People who have previously been diagnosed with a brain tumour other than a meningioma
  • People who have received a radioactive (radionuclide) therapy within the past 30 days
  • People who have received a type of cancer therapy targeting blood vessel growth (anti-VEGF therapy) within the past 6 weeks
  • People who are unable to tolerate the positioning and treatment involved in focused radiation therapy
  • People who are unable to give informed consent
  • People who are pregnant or breastfeeding
  • Women of reproductive potential who are not willing to use effective contraception for at least 6 months after radiation treatment
  • Men of reproductive potential who are not willing to use effective contraception for at least 3 months after radiation treatment
  • People who are unlikely to follow the study procedures and attend required follow-up appointments

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 28 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: Susanne Rogers, MD PhD, Kantonsspital Aarau, Radio-Onkologie-Zentrum Mittelland

Phone: +41 62 838 57 26

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
Susanne Rogers
Registry
ClinicalTrials.gov
Start date
29 July 2022
Est. completion
30 December 2028

Where this trial is recruiting

🇦🇹 Austria 🇩🇪 Germany 🇨🇭 Switzerland

Primary endpoints

Leptomeningeal disease

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: 28 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