Data Collection of Normal Tissue Toxicity for Proton Therapy for Pediatrics

Status unconfirmed

Conditions studied: Pediatric Cancer

In brief

The goal of this research study is to collect information on the side effects of proton therapy and the details of proton treatment plans so that researchers can develop a method to predict the risk of side effects and to improve the planning and delivery of proton treatment for patients in the future.

Key facts

Study ID

NCT01502150

Run by

M.D. Anderson Cancer Center

People needed

798

Starts

2005-06-16

Expected to finish

2021-06-01

Last updated by the study team

2019-05-10

Who can join

Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All patients under the age of 18 who are treated with PBT will be eligible to participate in this trial.
• Signed informed consent must be obtained from the patient or patient's representative prior to study enrollment.

You may not qualify if…

• Pregnant females are not eligible.
• Patient or patient's parent or legal guardian representative is unable or unwilling to give informed consent.

Where it is running

• University of Texas MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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