NCT07162324Not yet recruiting
A Multicenter, Prospective Study for Glioblastoma Patients
Summary
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.
Inclusion criteria
• Adult patients (\>18 years of age) with • Glioblastoma based on radiographic features, • Patients that consent for study participation.
Exclusion criteria
• Non adult patients, • Patients that do not consent for participation in this study, • Patients with other CNS tumors
Contacts
The trial team's contact details are shown on request.
See the official trial record- Status
- Not yet recruiting
- Phase
- —
- Study type
- Observational
- Countries
- Switzerland, United States, Greece
- Sponsor
- Larissa University Hospital(Other)
- Protocol no.
- 27446
- Conditions
- Glioblastoma
- Interventions
- —
Collaborators
University of Thessaly, University of California, San Francisco, University of Bern
Locations · 3
- Bern, SwitzerlandInselspital University Hospital of BernNot yet recruiting at this site
- San Francisco, United StatesUCSF Weil Institute for NeurosciencesNot yet recruiting at this site
- Larissa, GreeceUniversity Hospital of LarissaNot yet recruiting at this site
In total, worldwide, all 3 sites listed in the registry are planned; recruitment has not opened yet.
Site status per the ClinicalTrials.gov registry (last update posted: September 9, 2025).
This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.
See also
Other versions
These results are indicative and do not replace medical advice — discuss them with your doctor.