Global effort to unlock secrets of rare childhood cancer

NCT ID NCT00700414

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study collects medical and family history from children and teens with adrenocortical tumors, a rare cancer. Researchers also study tumor samples to learn about genetic factors like the TP53 gene. The goal is to better understand the disease and improve care worldwide.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to
If successful, this registry could help doctors better understand and treat this rare childhood cancer, potentially improving future outcomes.
What could go wrong
This is an observational registry, not a treatment trial. It collects information but does not test any new therapy, so direct benefits to participants are unlikely.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

Locations

  • All Children's Hospital/St. Petersburg Hospital

    COMPLETED

    St. Petersburg, Florida, 33701, United States

  • Cook Children's Medical Center

    COMPLETED

    Fort Worth, Texas, 76104, United States

  • St. Jude Children's Research Hospital

    RECRUITING

    Memphis, Tennessee, 38105, United States

    Contact Email: •••••@•••••

  • Stanford University

    COMPLETED

    Stanford, California, 94305, United States

  • The Children's Medical Center

    RECRUITING

    Dayton, Ohio, 45404, United States

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