Skip to content

LOGGIC Core BioClinical Data Bank

LOGGIC Core BioClinical Data Bank - LOGGIC Core

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00019035
Enrollment
5000
Registered
2019-11-29
Start date
2019-04-05
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Grade Glioma D33 D43

Interventions

Group 1: From samples taken during the routine (tumor tissue and blood), a molecular fingerprint of the tumor is generated by DNA methylation profile and RNA sequencing. Using this data, it is possibl

Sponsors

Hopp Kindertumorzentrum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 20 Years

Inclusion criteria

Inclusion criteria: - Age < 21 years. - Histologically verified LGG Exceptions (i.e. MRI based diagnosis) can be accepted only where a biopsy would pose an unacceptable risk to damage of eloquent brain structures. - Primary diagnosis or at relapse/progression - At primary diagnosis: - Histologically verified low-grade glioma / glioneuronal tumour WHO grade I or II. - Fresh frozen and paraffin tumour material together with blood available for molecular diagnostics. -At relapse/progression: -Fresh frozen and paraffin tumour material together with blood available for molecular diagnostics from primary diagnosis and/or current episode (preferably) of relapse/progression. - No exceptions for the submission of fresh frozen and paraffin tumour material with blood - In case that the date of diagnosis is earlier than the start of LOGGIC Core in a country, submission of fresh frozen and paraffin tumour material together with blood is mandatory with no exceptions (in other words, one can include “retrospective cases” only if material is available). - Before patient registration, written informed consent, including data and tumour material transfer, must be given according to ICH/GCP, and national/local regulations. - Residency in one of the participating countries of LOGGIC Core.

Exclusion criteria

Exclusion criteria: No LGG

Design outcomes

Primary

MeasureTime frame
Establishment of a molecular and clinical data base for pediatric low grade glioma

Secondary

MeasureTime frame
To collect molecular tumour characteristics of LGG patients for exploratory analysis of biomarker and clinical outcome.

Countries

Australia, Austria, Belgium, Czechia, Denmark, Finland, Germany, Greece, Hungary, Ireland, Italy, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom

Contacts

Public ContactCarina Bodden

Hopp Kindertumorzentrum Heidelberg

carina.bodden@kitz-heidelberg.de+496221564780

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026