Caring registry study for children and young people with cancer
Part of Blood & lymphatic, Brain & nervous system, Cancer, Immune system & allergy, Kidney & urinary, Skin, Women’s health & pregnancy clinical trials.
This study keeps a careful record of children, teens, and young adults with cancer (and some related growths) and may follow them over time. It helps researchers better track outcomes and future contact so care can improve.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You (or your parent/guardian) can join within 6 months of your first diagnosis or after a later relapse or return of cancer
- You are 25 or younger when you were first diagnosed (unless you are being screened for a specific COG treatment study with a higher age limit)
- Your diagnosis is a type of tumor or cancer that fits the study’s list (including most malignant cancers, some borderline/carcinoma-in-situ cases, and all central nervous system and kidney neoplasms)
- You may also qualify for certain specific “benign” or “borderline” conditions (like teratomas or Langerhans cell histiocytosis)
- A parent/guardian or you must sign the study consent form (and consent for extra bone marrow is recommended if that procedure is done first)
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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