Clinical Trials in the Netherlands / NCT06183983
Recruiting Not applicable

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

NCT06183983 · tracked via the Priya Life Science Netherlands tracker
Phase
Not applicable
Started
2024-01-03
Last updated
2025-06-12

Condition(s) studied

Glioblastoma

Investigational drug(s) / intervention(s)

Extended or additional MRI-scan (with contrast) prior to radiotherapy

Extended or additional MRI-scan (with contrast) prior to radiotherapy: The MRI-protocol before radiotherapy is extended with 20 minutes. Patients who would not have received an MRI-scan prior to radiotherapy, will get an extra MRI-scan when participating.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Criteria: * Contraindication for (3 Tesla) MRI; * Contraindication for use of gadolinium-based contrast agent (e.g. subject having renal deficiency or known allergy); * Referred for treatment of recurrent glioblastoma; * Previous radiotherapy to the brain; * Unable to give informed consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Erasmus Medical Center Rotterdam South Holland Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06183983 on ClinicalTrials.gov ↗ ← All trials in the Netherlands