Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06719440

Impact of Reducing the Irradiation Volume on Survival, Toxicity, and Quality of Life in Patients With Glioblastoma Treated With Radiochemotherapy: a Prospective Multicenter Randomised Study

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - During radiochemotherapy treatment period

Participants receive radiotherapy with either a reduced irradiation volume (CTV=10mm) or standard irradiation volume (CTV=15mm) along with chemoradiotherapy.

Follow-up

Duration - Up to 2 years after treatment

Participants are monitored for survival, neurocognitive functioning, radiation-induced toxicity, health-related quality of life, progression-free survival, pattern of recurrence, and anti-edema therapy effects.

Assessments at baseline, 1 month after radiotherapy, and at 1 year; ongoing monitoring until 2 years

Trial Site Locations

Total: 23 locations

1

Olv Azorg

Aalst, Belgium, 9300

Not Yet Recruiting

2

EpiCURA

Baudour, Belgium, 7331

Actively Recruiting

3

AZ Sint Jan

Bruges, Belgium, 8000

Actively Recruiting

4

Institut Jules Bordet

Brussels, Belgium, 1070

Not Yet Recruiting

5

UZ Brussel

Brussels, Belgium, 1090

Not Yet Recruiting

6

Cliniques universitaires Saint-Luc

Brussels, Belgium, 1200

Actively Recruiting

7

Ziekenhuis Oost-Limburg (ZOL)

Genk, Belgium, 3600

Actively Recruiting

8

AZ Sint-Lucas

Ghent, Belgium, 9000

Actively Recruiting

9

UZ Gent

Ghent, Belgium, 9000

Not Yet Recruiting

10

Grand Hôpital de Charleroi

Gilly, Belgium, 6060

Actively Recruiting

11

JESSA Ziekenhuis

Hasselt, Belgium, 3500

Actively Recruiting

12

AZ Groeninge

Kortrijk, Belgium, 8500

Actively Recruiting

13

Chu Helora

La Louvière, Belgium, 7100

Actively Recruiting

14

UZ Leuven

Leuven, Belgium, 3000

Actively Recruiting

15

CHU Liège

Liège, Belgium, 4000

Actively Recruiting

16

AZ Sint Maarten

Mechelen, Belgium, 2800

Actively Recruiting

17

Hôpital André Vésale - HUmani

Montigny-le-Tilleul, Belgium, 6110

Actively Recruiting

18

CH Mouscron

Mouscron, Belgium, 7700

Not Yet Recruiting

19

CHU UCL Namur - Sainte Elisabeth

Namur, Belgium, 5000

Actively Recruiting

20

AZ Delta

Roeselare, Belgium, 8800

Actively Recruiting

21

Cliniques de l'Europe

Uccle, Belgium, 1180

Actively Recruiting

22

CHR Verviers

Verviers, Belgium, 4800

Actively Recruiting

23

ZAS Augustinus

Wilrijk, Belgium, 2610

Actively Recruiting

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Research Team

D

Dario Di Perri, MD

C

Chloë De Laet

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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