Recruiting NCT06953245
Collecting Patient-Reported Experiences With Radiation Dermatitis in Breast Cancer Patients Undergoing Radiotherapy
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Non-Interventional Study.
- Who it may be relevant to
- Registry conditions: Breast Carcinoma. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This study evaluates patient-reported experiences of radiation dermatitis in patients with breast cancer undergoing radiotherapy.
Interventions
- Other Non-Interventional Study
Non-interventional study
Primary outcome measures
- Patient experiences with radiation dermatitis [Time frame: Baseline (at enrollment)]
Eligibility criteria
Inclusion criteria
- Adults ≥ 18
- Patients diagnosed with breast cancer
- Currently undergoing or recently completed radiotherapy
- Willing to provide verbal/oral consent
- Willing to be recorded as they are answering the survey questions
Exclusion criteria
- Persons < 18
- Inability to provide verbal consent
- Non-English speakers (unless translations are available)
- Not willing to be recorded
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
United States · 1 center
- Mayo Clinic in Rochester — Rochester
Identifiers
NCT: NCT06953245 · ROR2431 · NCI-2025-01198 · 24-007996 · ROR2431