Enhancing Skin Appearance and Quality of Life in Breast Cancer Survivors on Aromatase Inhibitor Therapy

ConditionsAnatomic Stage 0 Breast Cancer AJCC v8 Anatomic Stage I Breast Cancer AJCC v8 Anatomic Stage II Breast Cancer AJCC v8 Anatomic Stage III Breast Cancer AJCC v8 Breast Adenocarcinoma Estrogen Receptor-Positive Breast Carcinoma Progesterone Receptor-Positive Breast Carcinoma

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexFemale

Age18+

SponsorMayo Clinic

About this trial

This study evaluates changes in skin quality and self-esteem among breast cancer patients who are initiating aromatase inhibitor therapy.

Eligibility criteria

Qualifiers

* Female ≥ 18 years

Postmenopausal women suitable to receive aromatase inhibitor as per physician's discretion

Histologically confirmed adenocarcinoma of the breast stage 0-III with estrogen receptor (ER) and/or progesterone receptor (PR) positive per American Society of Clinical Oncology (ASCO)/ College of American Pathologists (CAP) guideline and any human epidermal growth factor receptor 2 (HER2)

Patients must not have received any prior chemotherapy or endocrine therapy for their current breast cancer. Patients who received tamoxifen or raloxifene or another agent for prevention of breast cancer may be included

Disqualifiers

* Patients who have previously taken AIs

Patients using prescription tretinoin, neurotoxin injections, fillers, facial lasers, microneedling, or facials within 6 months of study consent

Trial design

Treatments tested in this trial

Non-Interventional Study

Treatment groups

35 Participants

are divided into 1 treatment group

Locations

Mayo Clinic in Florida32224-9980, JacksonvilleFlorida, United States

Sponsors and collaborators

Mayo Clinic

Lead sponsor

Source ClinicalTrials.gov