Under construction – not a live service
Sign in
Taking people in NetherlandsNo phase

Tests advanced MRI scans to guide radiotherapy in brain tumor patients

Tests extra MRI scans before radiotherapy in adults with glioblastoma, a brain tumor.

Plain-language title generated from the registry record
Registry title: Hitting the Mark: Introducing State-of-the-art MRI for Precision Radiotherapy of Glioblastoma

Key facts

Where
Rotterdam, NetherlandsSee the site

Where in Netherlands

  • Erasmus Medical CenterRotterdam, NetherlandsTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Erasmus Medical Center
Trial code
NCT06183983
Record updated
12 June 2025
Original description
The goal of this prospective cohort study is to assess the potential of advanced MRI for improved radiotherapy target delineation in patients diagnosed with glioblastoma. The main questions it aims to answer are:Read full original descriptionShow less

Hitting the Mark: Introducing State-of-the-art MRI for Precision Radiotherapy of Glioblastoma

The goal of this prospective cohort study is to assess the potential of advanced MRI for improved radiotherapy target delineation in patients diagnosed with glioblastoma. The main questions it aims to answer are:

* How does the coverage of the recurrence volume by a radiotherapy plan based on advanced MRI compare to the coverage by the clinical radiotherapy plan? * How does the distribution of the dose to organs at risk by a radiotherapy plan based on advanced MRI compare to the distribution by the clinical radiotherapy plan?

Participants will undergo an extended MRI-protocol prior to radiotherapy. This extended MRI-protocol includes the clinical brain tumor imaging protocol plus additional advanced MRI-sequences. Radiation treatment and patient follow-up will occur according to the clinical standard.

Inclusion: Written informed consent; Adult (18 years or older); Diagnosed with IDH-wildtype glioblastoma, as confirmed by pathology including molecular analysis post resection/biopsy; Referred to the outpatient clinic of the Dept. of Radiotherapy to undergo standard treatment with radiotherapy (30x2 Gy or 15x2.67Gy or 10x3.4Gy).

Exclusion: Previous radiotherapy to the brain; Contraindication for use of gadolinium-based contrast agent (e.g. subject having renal deficiency or known allergy); Contraindication for (3 Tesla) MRI; Referred for treatment of recurrent glioblastoma; Unable to give informed consent.

ClinicalTrials.gov NCT06183983