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Study identifier: NCT06483477 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Dermatitis During Adjuvant Irradiation for BREAst Cancer:

Condition: Breast Cancer Female  ·  Sponsor: University Hospital Schleswig-Holstein

PhaseNA
Planned participants268
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

In the randomized DAI-BREAC trial, a reminder app will be prospectively tested that reminds breast cancer patients four times each day to perform the required skin care. This will likely contribute to the reduction of grade ≥2 radiation dermatitis in these patients. A total of 268 patients will be randomized to receive standard skin care supported by a reminder app (Arm A) or standard skin care alone (Arm B). Stratification will be done using the three factors treatment volume, radiation boost, and at least one risk factor of dermatitis. Secondary aims include pain (radiation fields), patient satisfaction with the reminder app (Arm A only), impact of the app on the use of health technology (Arm A only), and benefit from support by staff members of the treating Department of Radiation Oncology and/or the UKSH academy regarding the use of the app (Arm A only).

This description comes directly from the study's public registry record.

Talk to the study team

Dirk Rades, MD, FASTRO  ·  0049-451-500  ·  DIRK.RADES@UKSH.DE

Carlos A. Narvaez-Wolf, MD  ·  0049-451-500  ·  Carlos.Narvaez-Wolf@uksh.de

Always discuss trial participation with your own doctor first.

Locations (5)

Vejle Hospital, University Hospital of Southern DenmarkVejle, Southern Denmark, DenmarkNot Yet Recruiting
Medical Practice for Radiotherapy and Radiation OncologyHanover, Lower Saxony, GermanyNot Yet Recruiting
Medical School Hamburg, Schwerin CampusSchwerin, Mecklenburg-Vorpommern, GermanyNot Yet Recruiting
Malteser Hospital St. FranziskusFlensburg, Schleswig-Holstein, GermanyNot Yet Recruiting
Department of Radiation Oncology, University of Lübeck and University Medical Center Schleswig-HolsteinLübeck, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT06483477