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Rare Tumours in Children and Adolescents (STEP)

Recruitingn/aAges 1 Day - 18 YearsAllUniversity Hospital Tuebingen
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In plain words

What the trial is, and whether it could suit you

The aim of the STEP registry is to collect and evaluate experience and data on the diagnosis and treatment of rare childhood tumors in order to use the knowledge gained to improve the treatment prospects for our patients. The rarity of a disease should not be a disadvantage for the young patients.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Diagnosis of a rare solid tumor * Age at diagnosis: Neonatal period to 18 years (In the case of young adults, registration in the database and/or referral to advisory contact persons within the framework of the competence network can take place upon request and after declaration of consent.) * Information, education, written consent of the patient or the guardian * Not recorded in any of the existing clinical studies/ registers of the German Society for Pediatric Oncology and Hematology (GPOH) Exclusion Criteria: * Registration of the tumor diagnosis in a prospective therapy study/ another clinical registry of the GPOH * Lack of information, explanation and/or written consent of the patient or the legal guardian.
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What it tests

  • Data collection
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Where

1 site
University Hospital Tübingen
Tübingen, Germany
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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