Clin2
NCT07596212Possibly a fitNot yet recruiting

Testing a Drug to Help with Sexual Side Effects from Breast Cancer Treatment

Early-stage Breast CancerHypoactive Sexual Desire DisorderHormone Receptor Positive Breast CarcinomaBreast Cancer

Treatments studied

Part of Cancer, Mental health, Skin clinical trials.

This study tests whether a medication called bupropion can help women with hormone receptor-positive breast cancer who are taking aromatase inhibitors (drugs that block estrogen) but experiencing low sexual desire as a side effect. The goal is to see if this approach improves both tolerance to the cancer medication and quality of life.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
100 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have been diagnosed with early-stage hormone receptor-positive breast cancer (stage I–III) that has been surgically removed
  • You have completed all planned cancer treatments (surgery, radiation, and/or chemotherapy if needed) before starting this study
  • You are experiencing low sexual desire as a side effect of aromatase inhibitor treatment
  • You are able to swallow oral medication and willing to return to the clinic for follow-up visits
  • You are not pregnant, not breastfeeding, and willing to use birth control during the study and for 30 days after it ends
  • You do not have a history of certain mental health conditions, seizures, or eating disorders

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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