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NCT02686229 Clinical Trial

Registry Study on Epidemiological and Biological Disease Profile as Well as Clinical Outcome in Patients With Low Grade Gliomas

Glioma Clinical Trial

— LoG-Glio  

Official title:
Registry Study on Epidemiological and Biological Disease Profile as Well as Clinical Outcome in Patients With Low Grade Gliomas: The LOG-Glio-Project

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02686229
Other study ID # LoG-Glio
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 15, 2015
Est. completion date December 2036

Study information
Verified date May 2023
Source University of Ulm
Contact Jan Coburge, MD
Phone 082219628858
Email jan.coburger@uni-ulm.de
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The LoG-Glio-Registry is based on a network of german hospitals gathering radiological, clinical, epidemiological and molecular data on all patients diagnosed with a low grade glioma.

Recruitment information / eligibility
Status Recruiting
Enrollment 300
Est. completion date December 2036
Est. primary completion date December 31, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with radiological suspected diagnosis of a low grade glioma - Age = 18 years. There is no upper age limit. Exclusion Criteria: - Severe neurological or psychiatric disorder interfering with ability to give an informed consent - No consent for registration, storage and processing of the individual disease characteristics and course as well as information of the family physician about study participation - No consent for bio-banking of patient's biological specimens and performance of analyses on stored material.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• no interventions

Locations
Country Name City State
Germany University of Ulm Ulm

Sponsors (2)
Lead Sponsor Collaborator
University of Ulm Charite University, Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Progression-free survival (PFS) 5yrs
Primary Overall survival (OS) 15yrs
Secondary Extent of tumor resection calculated based on volumetric assessement of tumor in cm³ and residual tumor in pre and postoperative MRI 3yrs
Secondary Quality of life (QoL) assessed by the EORTC QLQ C-30/BN-20. (European Organisation for Research and Treatment of Cancer Quality of Life Questionaire C-30 5yrs
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