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Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06719440

Study of Reduced Radiation Area on Survival and Quality of Life in Glioblastoma Patients Undergoing Radiochemotherapy

Led by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Updated on 2026-02-27

347

Participants Needed

23

Research Sites

N/A

Total Duration

On this page

Sponsors

C

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Lead Sponsor

B

Belgium Health Care Knowledge Centre

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a new approach to radiotherapy for patients with glioblastoma, a common and aggressive brain tumor. This trial aims to determine if focusing radiation treatment more precisely by reducing the usual safety margin can safely decrease side effects and improve quality of life. Despite current treatments involving surgery, radiotherapy, and chemotherapy, survival remains limited and quality of life is often impaired for these patients. The study compares two radiotherapy approaches one with the standard irradiation volume including a 15mm safety margin around the tumor, and another with a reduced 10mm margin to limit the amount of healthy brain tissue exposed. Both groups receive chemoradiotherapy as part of their treatment. This national multicenter trial will randomize patients to either the standard or reduced radiotherapy volume to assess outcomes. Participants will be followed for up to two years with regular assessments of overall survival, neurocognitive function, treatment-related toxicity, quality of life, disease progression, and recurrence patterns. Evaluations include baseline measurements and follow-ups at one month and one year after radiotherapy. Researchers will also monitor use of anti-edema therapy during the study. The total participation duration and study procedures are designed to monitor safety and the impact of the radiation volume on patient well-being.

CONDITIONS

Brief Title

Achieving a Better Outcome Through Limiting the Glioblastoma Clinical Target Volume

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants capable of giving informed consent
  • Age >= 18 years
  • WHO performance status 0-2
  • Newly diagnosed glioblastoma confirmed by biopsy or resection
  • Indication for chemoradiotherapy confirmed by multidisciplinary tumour board
Not Eligible

You will not qualify if you...

  • Participation in a competing trial
  • Known contraindication to undergo MRI scans

Research Team

D

Dario Di Perri, MD

C

Chloë De Laet

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