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NCT05500612Recruiting

MRI Hypoxia Study for Glioblastoma Multiforme (GBM) Radiation Therapy

Magnetic Resonance Imaging of Hypoxia for Radiation Treatment Guidance in Glioblastoma Multiforme (MANGO)

Source: ClinicalTrials.gov · Last updated 19 May 2026

Brief summary (registry, in English)

This study is designed to evaluate the role of Oxygen Enhanced (OE) Magnetic resonance imaging (MRI) and Blood Oxygenation Level Dependent (BOLD) MRI in detecting regions of hypoxic tumour and to evaluate their use as imaging methods to selectively deliver targeted radiotherapy to regions of aggressive disease.

Status (registry)
Recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
9 Aug 2022
Start date
Aug 2024
Primary completion date
Dec 2026
Lead sponsor
University of Sydney
Diseases
Glioblastoma
NCT number
NCT05500612

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From Aug 2024 to the primary completion date, Dec 2026
  • 2 sites in 1 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

  • Patients who have received anti - vascular endothelial growth factor (anti-VEGF) monoclonal antibody therapy the 3 months prior to recruitment
  • Patients taking carbonic anhydrase inhibitors (Acetazolamide)
  • Any implant, foreign body, 3 Tesla (3T) MRI incompatible device, or other contraindication to MRI imaging.

Other illness

  • Patients with a history of psychological illness or condition such as to interfere with the patient's ability to understand the requirements of the study.
  • Patients with significant cardiac or pulmonary disease including cardiac arrythmias or Chronic Obstructive Pulmonary Disease (COPD) that are unable to tolerate high flow O2 for oxygen contrast.
  • History of glaucoma

Lab values

  • Patients with a history of severe renal disease(s) (eGFR \<20) that cannot tolerate gadolinium chelate contrast agents.

Other

  • Women lactating, pregnant or of childbearing potential who are not willing to avoid pregnancy during the study
  • Geographically remote patients unable to agree to imaging schedule

Who the study is looking for

  • Suspected high-grade glioma (HGG) / glioblastoma multiforme (WHO grade IV) at initial radiological examination
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2
  • Available for scanning on two separate days

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
North Shore Private Hospital
Coordinator of this site? Confirm its status
St LeonardsAustraliaNot yet recruiting
Royal North Shore Hospital
Coordinator of this site? Confirm its status
St LeonardsAustraliaRecruiting

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