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ACTIVE NOT RECRUITING
NCT06443359
NA

Hypofractionated Regional Nodal Irradiation in Breast Cancer

Sponsor: Corewell Health East

View on ClinicalTrials.gov

Summary

This is a prospective clinical trial designed to evaluate the efficacy and safety of hypofractionated regional nodal irradiation in breast cancer patients. After enrollment, participants will be stratified into 2 Groups based on the extent of axillary surgery. Participants will complete activities and assessments at baseline, and after completion of treatment at 1-2 weeks, 3 months, 6 months, 1 year, 2 year, and 3 years following completion of treatment.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

56

Start Date

2018-11-13

Completion Date

2027-07

Last Updated

2025-06-11

Healthy Volunteers

No

Conditions

Interventions

RADIATION

hypofractionated radiation

All patients will receive a dose of 42.56 Gy in 16 daily fractions to the whole breast or chest wall and regional lymph nodes. A boost dose of 10 or 12.5 Gy in 4 or 5 daily fractions of 2.5 Gy, respectively, will be administered to either the lumpectomy cavity or mastectomy scar, as appropriate.

Locations (3)

Corewell Health Dearborn Hospital

Dearborn, Michigan, United States

Corewell Health William Beaumont University Hospital

Royal Oak, Michigan, United States

Corewell Health Beaumont Troy Hospital

Troy, Michigan, United States