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

Study category: Cancer

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Description

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

Details
Age

Adult

Eligibility

1. Patient must have histologically confirmed ductal carcinoma in situ (DCIS) in a single breast (presence of lobular carcinoma in situ (LCIS) or other benign breast disease in addition to DCIS is acceptable) 2. Patient must have the DCISionRT™ Test ordered during routine patient care 3. Patient must be planning to undergo breast conserving surgery 4. Patient must be eligible to receive radiation and/or systemic treatment 5. Patient must be greater than 25 years old 6. Patient must have been diagnosed with DCIS within 120 days of consent 7. Patient must be able to provide informed consent

Phase

Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.

Type of Study

Diagnostic

Locations

Memorial Hospital Central
Memorial Hospital North

Principal Investigator
Jane Ridings

Jane Ridings

Study ID

Protocol Number: 20-1420

More information available at ClinicalTrials.gov: NCT03448926

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