Under construction – not a live service
Sign in
Taking people in ItalyNo phase

Studying Tumour Cells and Patient Data to Guide Glioblastoma Care

Analyses tumour stem cells, immune markers and patient data in adults with glioblastoma.

Plain-language title generated from the registry record
Registry title: Stem Cell Analysis, Omics (Including Immunomics) and Artificial Intelligence in Glioblastoma

Key facts

Where
Rome, ItalySee the site

Where in Italy

  • Fondazione Policlinico Universitario A. Gemelli IRCCSRome, ItalyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Trial code
NCT05941234
Record updated
13 March 2025
Original description
The study aims at:Read full original descriptionShow less

Improving Personalised Glioblastoma Care by Stem Cell Analysis, Omics (Including Immunomics) and Artificial Intelligence Approaches

The study aims at:

1. Perform a multilayer analysis relying on tight integration of in-depth multi-omics approaches with clinical data to discover immune markers, with attention to age and sex differences, predicting prognosis and defining key life/environmental elements, to guide AI-driven personalised treatments and ensure improved care and QoL of glioblastoma patients. 2. To deepen glioblastoma knowledge through the study of glioblastoma stem cell cultures and to assess the sensitivity of glioblastoma stem cell cultures to a number of chemotherapeutics in different experimental conditions. 3. To create a comprehensive, stakeholder-generated guidelines for the ethical use of patient data for artificial intelligence-assisted prediction systems in glioblastoma, including an online, easily accessible patient information brochure to increase patient empowerment in the field.

Inclusion: To be enrolled in the study patients must:; Have a radiological diagnosis of supratentorial glioblastoma, or; Have a radiological diagnosis of first recurrence of a primary supratentorial glioblastoma (for which a formal histopathologic diagnosis of glioblastoma had made at first surgery), according with RANO criteria; Be a candidate to neurosurgery for glioblastoma at the Operational Unit of Neurosurgery Fondazione Policlinico Gemelli IRCCS; Be of an age of 18 years or above; Provide written informed consent for participation to the study.

Exclusion: Have not enough pathological material removed at surgery available both for mandatory routine histopathological diagnosis and for the present study, as judged by the Principal Investigator; To be enrolled in the study patients must not:; Have not a definitive pathological diagnosis of a primary supratentorial glioblastoma, according with 2021 World Health Organization classification.

ClinicalTrials.gov NCT05941234