Biological Collection of Brain Tumors (GLIOLI)

January 16, 2026 updated by: Hospices Civils de Lyon

Biological Collection of Brain Tumors - GLIOLI Collection

The objective of this study is to build a collection of biological samples from patients with brain tumors.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

500

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patient with brain tumor

Description

Inclusion Criteria:

  • Patient whose diagnosis of brain tumor has been confirmed.
  • Adult patients, from 18 years old and without upper age limit
  • Patient affiliated to a social security scheme or equivalent.
  • Patient able to consent, having dated and signed an informed consent

Exclusion Criteria:

  • Pregnant or breastfeeding women
  • Patient under guardianship or curators.
  • Persons deprived of their liberty by a judicial or administrative decision

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
brain tumors

blood and/or collection

Only once :

  • 1 tube of blood of 4 mL on dry tube with or without gel,
  • 2 tubes of blood of 4 mL on EDTA tube, If CSF collected for diagnosis is available, it can be sent for storage in the collection.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
number of biological samples
Time Frame: 10 years
number of biological samples
10 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 22, 2023

Primary Completion (Estimated)

November 22, 2033

Study Completion (Estimated)

November 22, 2033

Study Registration Dates

First Submitted

October 3, 2022

First Submitted That Met QC Criteria

October 5, 2022

First Posted (Actual)

October 7, 2022

Study Record Updates

Last Update Posted (Actual)

January 20, 2026

Last Update Submitted That Met QC Criteria

January 16, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Brain Tumor

Clinical Trials on blood and/or csf collection

Subscribe