A Prospective Registry Study to Evaluate the Effect of the DCISionRT Test on Treatment Decisions in Patients With DCIS Following Breast Conserving Therapy

Investigator: Sandra Templeton, MD

Study Coordinator: Pej Hemati

Status: Enrolling

ClinicalTrials.gov Number: NCT03448926

Phone: 713.441.3926

Protocol Number: Pro00022187

Description

This is a prospective cohort study for patients diagnosed with ductal carcinoma in situ (DCIS) of the breast. The primary objective of the study is to create a de-identified database of patients, test results, treatment decisions and outcomes that can be queried to determine the utility of the DCISionRT™ test in the diagnosis and treatment of ductal carcinoma in situ of the breast.
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