Status:

TERMINATED

Combined Optical and Infrared Imaging for Early Prediction of Erythema During Breast and Chestwall Radiotherapy

Lead Sponsor:

Nova Scotia Health Authority

Conditions:

Breast Cancer

Eligibility:

FEMALE

Phase:

NA

Brief Summary

The aim of this study is to develop a computer model, based on photographs and heat images of patients' skin, to provide early prediction of painful reddening of the skin during radiotherapy treatment...

Detailed Description

There is currently no reliable tool to quantify and detect erythema of the skin during radiotherapy. This side-effect may lead to painful moist desquamation, and eventually permanent delayed side effe...

Eligibility Criteria

Inclusion

  • \- All female patients referred for adjuvant radiotherapy following breast conserving surgery/mastectomy.

Exclusion

  • Patients with known skin issues (e.g. dermatomyositis, rosacea)
  • Patients with excessive risk of skin recurrence, including T4d
  • Patients with locally advanced breast cancer.

Key Trial Info

Start Date :

July 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 14 2021

Estimated Enrollment :

7 Patients enrolled

Trial Details

Trial ID

NCT04363892

Start Date

July 1 2020

End Date

June 14 2021

Last Update

August 21 2024

Active Locations (1)

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Dalhousie University - Radiation Oncology Department

Halifax, Nova Scotia, Canada, B3H 4H7

Combined Optical and Infrared Imaging for Early Prediction of Erythema During Breast and Chestwall Radiotherapy | DecenTrialz