Plain-English translation of NCT07129317 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Johns Hopkins is building a registry — a detailed database — to track children who receive radiation therapy for brain tumors or sarcomas (cancers of bone or soft tissue). The registry will collect information about the exact dose of radiation each child receives, how they respond to treatment, any side effects they experience, and how they're doing over time. This information will help doctors improve radiation therapy and compare which types work best.
Radiation therapy is an important treatment for pediatric cancers, but doctors need better long-term data to understand which approaches work best and how to minimize side effects in children. This registry will help answer those questions so future children can receive the safest, most effective care possible.
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If you join, your medical team will record detailed information about your radiation therapy treatment, including the exact dose you receive and where it's aimed. You'll be asked to share information about your health, any side effects you experience, and your quality of life at various points during and after treatment. This information becomes part of the registry so researchers can study long-term outcomes and help improve care for other children in the future.
AI-generated summary from trial data · Jul 3, 2026 · Not medical advice
United States
Collaborators
Clark Charitable Foundation Inc.
Enrollment target
~5,000 participants
Started
October 2025
Primary completion
September 2035
Age range
0 Years – 26 Years
Last updated on clinicaltrials.gov in November 2025.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Ethan Arnone, BS
SKCCC Johns Hopkins Medical Institution
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.