Effects of vaginal administration of conjugated estrogens tablet on sexual function in postmenopausal women with sexual dysfunction: a double-blind, randomized, placebo-controlled trial

BMC Womens Health. 2020 Aug 12;20(1):173. doi: 10.1186/s12905-020-01031-4.

Abstract

Background: Female sexual dysfunction (FSD) is prevalent in women with genitourinary syndrome of menopause (GSM). Vaginal estrogen is effective GSM treatment. This study was primarily aimed to evaluate the effects of vaginal administration of conjugated estrogens tablet on postmenopausal FSD using the Female Sexual Function Index (FSFI). Secondary aims were to evaluate vaginal pH, Vaginal Maturation Value (VMV), Normal Flora Index (NFI) and Most Bothersome Symptoms (MBS) changes.

Methods: A double-blind trial was conducted in postmenopausal women with FSD (FSFI ≤26.55). Sixty-seven participants were randomized into two arms; vaginally administered conjugated estrogens tablet (0.625 mg, daily for 3 weeks then twice weekly for 9 weeks, n = 33), or placebo (n = 34).

Results: There was no significant improvement of FSFI observed in estrogens arm compared to placebo in each domain and overall index (p = 0.182). The estrogens significantly improved vaginal pH and VMV, toward more acidity (p = < 0.001), higher VMV (p = < 0.001) and more superficial cells (p = < 0.001). We observed no significant difference in NFI and MBS between arms (p = 0.282, 0.182).

Conclusion: We found no significant changes in FSFI, NFI, and MBS, but significant improvement in vaginal pH and VMV in postmenopausal women with FSD treated with vaginally administered conjugated estrogens tablet. Few side-effects were reported.

Trial registration: Thai Clinical Trial Registry identification number TCTR20180219001 , prospectively registered since 2018-02-19 11:33:21.

Keywords: Dyspareunia; Genitourinary syndrome of menopause; Hormonal therapy; Sexual dysfunction; The female sexual function index; Vaginal maturation index; Vaginal pH; Vulvovaginal atrophy.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intravaginal
  • Aged
  • Atrophy / drug therapy
  • Double-Blind Method
  • Dyspareunia / drug therapy*
  • Dyspareunia / pathology
  • Estrogens, Conjugated (USP) / administration & dosage*
  • Estrogens, Conjugated (USP) / therapeutic use
  • Female
  • Female Urogenital Diseases / drug therapy*
  • Humans
  • Middle Aged
  • Postmenopause / drug effects*
  • Prospective Studies
  • Tablets / administration & dosage*
  • Tablets / therapeutic use
  • Thailand
  • Treatment Outcome
  • Vagina / pathology
  • Vulva / drug effects*
  • Vulva / pathology

Substances

  • Estrogens, Conjugated (USP)
  • Tablets

Associated data

  • TCTR/TCTR20180219001