Fact CheckerSign in

NCT07670455Not yet recruiting

Brain Radiotherapy Imaging for High-grade Glioma Using Hypoxia Targeting Through Oxygen-Enhanced Response

Source: ClinicalTrials.gov · Last updated 30 Jun 2026

Brief summary (registry, in English)

High-grade gliomas (HGGs) are the most common type of brain cancer in adults. Life expectancy for patients with HGGs is low. Radiotherapy aims to cure the tumour, but this is hard because HGGs are resistant to treatment. Among the possible causes of resistance may be tumour cells with low-oxygen levels (hypoxia). The investigators know that hypoxia reduces tumour sensitivity to radiotherapy. Using a special imaging technique called oxygen-enhanced MRI (OE-MRI), the investigators can try to identify areas of the tumour with hypoxia. The investigators could then give those areas a higher dose of radiotherapy. This might improve tumour control. This study aims to see if OE-MRI can find low-oxygen areas in HGGs. The study will also assess whether higher radiotherapy doses can be simulated in these regions. Project summary: 1. Set up the OE-MRI process at Leeds Cancer Centre (LCC). OE-MRI settings will be tested on healthy volunteer participants to ensure the images are as good as possible. 2. Participant Imaging. Patient participants with HGG will be recruited to take part. OE-MRI will be used to image participants during their treatment and track low-oxygen areas before treatment, halfway through treatment and 3 months after treatment has finished. 3. Dose Escalation Assessment. Computer programs will be used to design radiotherapy treatments to test if higher radiation doses to the tumour's low-oxygen areas can better control the cancer. This will help understand if this targeted approach has potential benefits. This is modelling and will not alter routine clinical patient participant management.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
25 (estimated)
First submitted
19 Jun 2026
Start date
Sept 2026
Primary completion date
Aug 2028
Lead sponsor
The Leeds Teaching Hospitals NHS Trust
Diseases
Glioblastoma
NCT number
NCT07670455

What you commit to

  • Study type: Interventional
  • Planned participants: 25
  • From Sept 2026 to the primary completion date, Aug 2028
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants who have previously been treated with bleomycin (a chemotherapy used to treat some cancers including Hodgkin lymphoma and germ cell tumours).

Other illness

  • Participants with illness or condition which means they cannot understand the requirements of the study.
  • Participants with cardiac or pulmonary disease that are unable to tolerate the flow of oxygen delivered via a mask.

Other

  • Participants with any MRI contraindications including inability to lie flat in MRI scanner, claustrophobia and no foreign bodies, medical devices or other items which are considered an MRI contraindication.
  • Geographically remote patients unable to agree to imaging schedule.
  • Participants with contraindications to gadolinium-based contrast agent

Who the study is looking for

  • ≥18yrs.
  • Participants able to communicate with staff and safely comply with the study procedures.
  • Participants to provide informed written consent.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.