Registry Study for Proton Therapy Clinical Outcomes
This study is creating a national registry to track the health of people who receive proton therapy for cancer. Proton therapy is a special type of radiation treatment, and doctors want to learn more about its long-term effects. By joining, you would allow researchers to collect information about your health over many years after your proton therapy. This helps them understand how well proton therapy works for different conditions and if there are any long-term side effects. The main goal is to follow your health for a long time, starting at 6 months after treatment. Anyone receiving or seeking care at a participating Proton Therapy Center can join, as long as they agree to participate.
- Study design
- This is an observational study, meaning researchers will collect information about your health over time without giving you a specific treatment. The study plans to include 300 participants.
- What's involved
- You would allow researchers to maintain regular contact with you throughout your life to gather your current contact information and self-reported health status. They may also review your medical records.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed long-term, with initial follow-up measured at 6 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Registry Study for Proton Therapy Clinical Outcomes and Long-Term Follow-up
At a glance
Conditions
Where it's being run
3 sites across 3 statesStudy leadership
- James R Gray, M.D. · PRINCIPAL_INVESTIGATOR · Provision Center for Proton Therapy
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Long-term follow-up6 months
Maintaining regular, lifetime contact with subjects in order to obtain current identification , contact information, and self/parent-reported health status in order to obtain a better understanding of overall treatment strategies and patient benefits of treatment.