The Sarcoma Biology and Outcome Project
Recruiting now
Conditions studied: Sarcoma, Malignant Mesenchymoma, Sarcoma of Bone and Connective Tissue
In brief
SarcBOP - An interdisciplinary and translational registry SarcBOP aims to establish a database that integrates every aspect possibly relevant to sarcoma treatment and research. SarcBOP thus will not be limited to specific questions or patient groups, but instead will build a comprehensive database including clinical, pathologic, and radiologic information, multi-layered molecular data, and patient-reported outcomes, combined with a dedicated biobank for tissue samples and liquid biopsies. As the study integrates seamlessly with the clinical activities of the Heidelberg Sarcoma Center, the Molecular Diagnostics Program of NCT Heidelberg, including the NCT/DKTK MASTER Program, and with the NCT Trial Center, including the PMO Clinical Trials Program, SarcBOP will generate a comprehensive and continuously growing resource for clinicians, researchers, and, finally, patients.
Key facts
- Study ID
- NCT04758325
- Run by
- Prof. Dr. Richard F Schlenk
- People needed
- 3000
- Starts
- 2019-07-23
- Expected to finish
- 2032-12-31
- Last updated by the study team
- 2025-03-25
Who can join
Age: 12 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Suspected or proven diagnosis of soft-tissue or bone sarcoma (STBS)
- Age ≥12 years
- Ability to understand nature and individual consequences of the registry
- Written informed consent
- Subjects who are physically or mentally capable of giving consent
You may not qualify if…
- Severe neurological or psychiatric disorder interfering with the ability to give written informed consent
Where it is running
- National Center for Tumour Diseases, University Hospital Heidelberg — Heidelberg, Baden-Wurttemberg, Germany (enrolling)
Full record on ClinicalTrials.gov
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