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Study identifier: NCT06719440 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Achieving a Better Outcome Through Limiting the Glioblastoma Clinical Target Volume

Condition: Glioblastoma · Radiotherapy Side Effect  ·  Sponsor: Cliniques universitaires Saint-Luc- Université Catholique de Louvain

PhaseNA
Planned participants347
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objective of the BELGICA trial is to evaluate if radiotherapy could be given in a more focused manner in patients with glioblastoma in order to reduce side effects and improve quality of life. The glioblastoma (GBM) is the most common and aggressive tumour originating from the brain, affecting approximately 600 patients per year in Belgium. The treatment consists in surgical resection of the tumour (when feasible), followed by a combination of radiotherapy and chemotherapy. Despite multimodal treatment (surgery, radiotherapy, and chemotherapy), the life expectancy of patients with GBM remains limited, with an average survival of 12-18 months and only 5% of patients surviving more than 5 years. In addition to limited survival, most patients with GBM experience impaired quality of life, both because of the disease and treatments. Radiotherapy is a treatment where radiation is used to kill cancer cells. In GBM, radiotherapy is targeted at the tumour (or tumour bed if the tumour was resected) with a safety margin around it (the "Clinical Target Volume" or CTV) to account for potential microscopic spread of the tumour. The downside of this safety margin is that a substantial amount of brain tissue is irradiated, which can lead to treatment toxicity. Reducing the CTV margin would enable to decrease the volume of brain being irradiated and could thereby allow to reduce the side effects of brain irradiation. The BELGICA trial (Achieving a BEtter outcome through Limiting the Gl…

This description comes directly from the study's public registry record.

Talk to the study team

Dario Di Perri, MD  ·  +32 2 764 47 52  ·  dario.diperri@saintluc.uclouvain.be

Chloë De Laet  ·  +32 2 764 82 75  ·  Belgica.kce@saintluc.uclouvain.be

Always discuss trial participation with your own doctor first.

Locations (23)

Olv AzorgAalst, BelgiumNot Yet Recruiting
EpiCURABaudour, BelgiumRecruiting
AZ Sint JanBruges, BelgiumRecruiting
Institut Jules BordetBrussels, BelgiumNot Yet Recruiting
UZ BrusselBrussels, BelgiumNot Yet Recruiting
Cliniques universitaires Saint-LucBrussels, BelgiumRecruiting
Ziekenhuis Oost-Limburg (ZOL)Genk, BelgiumRecruiting
AZ Sint-LucasGhent, BelgiumRecruiting
UZ GentGhent, BelgiumNot Yet Recruiting
Grand Hôpital de CharleroiGilly, BelgiumRecruiting
JESSA ZiekenhuisHasselt, BelgiumRecruiting
AZ GroeningeKortrijk, BelgiumRecruiting

+ 11 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06719440