Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE®)
This site was designed to provide you with information about the PRO-CTCAE®, a patient-reported outcome measurement system developed by the National Cancer Institute to capture symptomatic adverse events in patients on cancer clinical trials.More About PRO-CTCAE
The National Cancer Institute’s PRO-CTCAE Measurement System was developed to capture symptomatic toxicity by self-report in adults, children and adolescents participating in cancer clinical trials.
Instruments & Form Builder
Download the full instruments, preview the item libraries using the Quick Guides, or use our Form Builders to produce a custom survey in any available language for your study.