Sexual Dysfunction Clinical Trial
Official title:
Impact of Lactate-containing Vaginal Lubricant on Sexual Dysfunction in Young Breast Cancer Survivors: Prospective Randomized Controlled Trial
The purpose of this study is to determine whether lactate-containing vaginal lubricant is effective in the treatment of young breast cancer survivors with sexual dysfunction.
Study scheme
- study arm: apply lactate-containing lubricants at the time of sexual intercourse and
before sleep at least 3 times per a week for 8 weeks
- control arm: placebo apply
Outcome measures
- Female Sexual function Index (FSFI-20): at 0 wk and at 8 wk
- vaginal maturation index: at 0 wk and 8 wk
- vaginal pH: at 0 wk and 8 wk
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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