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Clinical Trial Details Page

Electronic Patient Reporting of Symptoms During Cancer Treatment (PRO-TECT)

PRO-TECT (AFT-39)

Objective
Brief Summary:
The current study is designed to test nationally whether patients' outcomes and utilization of services can be improved through symptom monitoring via patient-reported outcomes between visits.
IRB Protocol Number
NCT03249090

Clinical Trial Categories

  • Breast Cancer
Contact
Nancy Burns at 919-784-7209
or Nancy.Burns2@unchealth.unc.edu
How to Participate

View eligibility criteria and additional study information

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