drugset / Trial / NCT06106529

REDucing Hot FLASHes in Women Using Endocrine Therapy.

NCT06106529

Phase 3 Recruiting 260 enrolled Reinier de Graaf Groep
RandomizedCrossoverOpen-labelTreatment

Summary

The goal of this randomized intrapatient cross-over study is to assess the efficacy of oxybutynin versus venlafaxine in reducing hot flashes in women using endocrine therapy after breast cancer. The objectives it aims to answer are: * To assess the efficacy of oxybutynin versus venlafaxine in reducing hot flashes in women using endocrine therapy after breast cancer * To assess side effects of oxybutynin versus venlafaxine. * To assess the personal preference of women for oxybutynin versus venlafaxine in reducing hot flashes. * To assess quality of life of women when reducing hot flashes in women using endocrine therapy after breast cancer. Participants will fill-out a patient diary during 15 weeks total on a daily basis and receive an (online) questionnaire three times total. Researchers will compare two groups (venlafaxine group versus oxubutynine group) to assess its efficacy concerning hot flashes.

Timeline

Start
2024-10-03
Primary completion
2029-01-01
Completion
2029-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxybutynin Small molecule 5 mg
Subject Venlafaxine Small molecule 75 mg