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Clinical Trial Summary

The objective of the International Rare Brain Tumor Registry (IRBTR) is to better understand rare brain tumors through the collection of biospecimens and matched clinical data of children, adolescents, and young adult patients diagnosed with rare brain tumors.


Clinical Trial Description

The International Rare Brain Tumor Registry (IRBTR) is a prospective observational study that will collect tumor samples and matched clinical and radiological data to better understand the outcomes of patients with rare brain tumors in particular: CNS sarcoma, BCOR, MN-1 altered tumors, and other unclassified rare brain tumors. Data collected include demographics, disease characteristics, treatment information, radiological imaging, and biospecimen collection if available ( tumor tissues Patients will be followed longitudinally to obtain outcome data. Data collection will continue for approximately 10 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05697874
Study type Observational [Patient Registry]
Source Children's National Research Institute
Contact Adriana Fonseca, MD
Phone 202-476-8399
Email afonsecash@childrensnational.org
Status Recruiting
Phase
Start date January 1, 2023
Completion date December 2033