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Impact of Aromatase Inhibitor Therapy on Glucose Homeostasis and Diabetes Risk

RecruitingObservational studyHealthy volunteers welcome

Who can join

All ages · Women · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Post-menopausal women with hormone receptor positive breast cancer, ductal carcinoma in situ (DCIS), or with other high risk breast conditions. Post-menopause will be defined as women who experience 12 months of amenorrhea or have undergone bilateral salpingo-oophorectomy.

  * 25 women who are planning to start or are within 6 months of starting treatment with aromatase inhibitors, after consultation in breast clinic and cancer center.
  * 25 women who will be starting Tamoxifen (comparative group)
  * 25 healthy post menopausal women will also be recruited.

Exclusion Criteria:

* Established diagnosis of diabetes
* Therapy with medications that could affect glucose metabolism
* Screening fasting glucose ≥ 126 mg/dl, and/or HbA1c ≥ 6.5%
* History of upper GI surgery that alters gastric emptying or causing malabsorption e.g., bariatric surgery, fundoplication

About the study

This study assesses the effect of hormone directed treatment for breast cancer on glucose metabolism.

What is being tested

Sponsor: Mayo Clinic · Participants: 81 · Started: Nov 16, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT06557057

Locations in the U.S.

MinnesotaMayo Clinic in Rochester, Rochester

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.