NCT07162324Pas encore en recrutement
A Multicenter, Prospective Study for Glioblastoma Patients
Résumé
Glioblastoma (GBM) is the most common and aggressive primary tumor of the adult central nervous system (CNS), with a poor prognosis and median overall survival ranging between 14 to 20 months despite advancements in diagnostic and therapeutic strategies. This prospective, observational, multicenter study aims to collect and analyze comprehensive data from GBM patients treated across selected centers in Europe and the United States, the investigators' centers included. Information will include demographics, imaging findings, molecular subtypes, clinical status, surgical strategies, postoperative management, complications, and follow-up data. Patients over 18 years old with radiographic evidence of GBM who provide informed consent will be included. Surgical interventions will vary, ranging from biopsy to supramaximal resections, based on individual patient and surgeon decisions. Key outcomes of interest include overall survival (OS) and progression-free survival (PFS). Secondary endpoints include perioperative complications, extent of resection (EoR), pre- and postoperative Karnofsky Performance Scores (KPS), hospital stay duration, and identification of risk factors influencing OS and functional outcomes. Patient monitoring will include standardized follow-up at one, three, and six months postoperatively, and quarterly thereafter or as clinically indicated. Statistical analysis will be conducted using R software, applying descriptive statistics, chi-square tests, logistic and linear regression, and assessing statistical significance at p \< 0.05. Results will also be expressed in odds ratios with 95% confidence intervals. This study seeks to define optimal surgical strategies based on patient-specific factors and contribute to improved, personalized treatment pathways for GBM management.
Critères d'inclusion
• Adult patients (\>18 years of age) with • Glioblastoma based on radiographic features, • Patients that consent for study participation.
Critères d'exclusion
• Non adult patients, • Patients that do not consent for participation in this study, • Patients with other CNS tumors
Contacts
Les coordonnées de l'équipe de l'essai s'affichent sur demande.
Voir la fiche officielle de l'essai- Statut
- Pas encore en recrutement
- Phase
- —
- Type d'étude
- Observationnelle
- Pays
- Suisse, États-Unis, Grèce
- Promoteur
- Larissa University Hospital(Autre)
- N° de protocole
- 27446
- Pathologies
- Glioblastoma
- Interventions
- —
Collaborateurs
University of Thessaly, University of California, San Francisco, University of Bern
Lieux · 3
- Bern, SuisseInselspital University Hospital of BernRecrutement pas encore ouvert dans ce centre
- San Francisco, États-UnisUCSF Weil Institute for NeurosciencesRecrutement pas encore ouvert dans ce centre
- Larissa, GrèceUniversity Hospital of LarissaRecrutement pas encore ouvert dans ce centre
Au total, dans le monde, les 3 centres listés au registre sont prévus ; le recrutement n'est pas encore ouvert.
Statut par centre selon le registre ClinicalTrials.gov (dernière mise à jour publiée : 9 septembre 2025).
Ce statut peut avoir changé et ne dit rien de votre éligibilité : avant toute démarche, vérifiez avec votre oncologue ou le centre.
Voir aussi
Autres versions
Ces résultats sont indicatifs et ne remplacent pas un avis médical — à discuter avec votre médecin.