Department of midwifery, Student Research Committee, Faculty of Nursing and Midwifery, Tabriz University of medical sciences, Tabriz, Iran.
Midwifery Department, Faculty of Nursing and Midwifery, Tabriz University of Medical Sciences, Tabriz, Iran.
BMC Pregnancy Childbirth. 2022 Jan 22;22(1):62. doi: 10.1186/s12884-022-04384-w.
Considering the importance of sexual function, high prevalence of sexual dysfunction (especially dyspareunia caused by atrophic vaginitis) in breastfeeding women, and lack of effective interventions, the present research aimed to determine the effect of oxytocin (OXT) vaginal gel on sexual function (primary outcome), sexual satisfaction, and depression (secondary outcomes) in the breastfeeding women.
This randomized triple-blind controlled trial was conducted on 64 breastfeeding women who referred to health centers in the city of Tabriz, Iran, in 2020-21. Participants were equally assigned to intervention/control groups using block randomization. 200 IU of OXT vaginal gel was given to the participants in the intervention group daily for eight week and the same protocol was carried out for the control group with placebo. Standard questionnaires of Female Sexual Function Index (FSFI), Edinburgh Postpartum Depression Scale (EPDS) and Sexual satisfaction scale for women (SSSW) were completed at baseline and 8 weeks after intervention. ANCOVA test was used to compare post-intervention mean score of the groups, adjusted for the baseline values.
After intervention, there was no statistically significant difference between groups in terms of mean total score of FSFI (Adjusted Mean Difference (AMD): 1.14; 95% Confidence Interval (95% CI): -1.28 to 9.16; P= 0.349) and sexual satisfaction (AMD: 5.01; 95% CI: -0.53 to 10.56; P= 0.075). However, there was statistically significant difference between the groups in terms of mean scores of sexual contentment (AMD: 1.56; 95% CI: 0.29 to 2.83; P = 0.017) and depression (AMD: -1.90; 95% CI: -1.27 to -2.54; P < 0.001). One participant in the OXT group and one participant in the placebo group reported mild uterine contraction and one person in the placebo group reported vaginal burning sensations.
No evidence was found for the effects of OXT gel in the improvement of FSFI, even though, OXT significantly improved sexual satisfaction in the domain of contentment, and improved the symptoms of depression in comparison to the placebo group. However, a definite conclusion requires more research in this regard.
the Iranian Registry of Clinical Trials (IRCT), code: IRCT20120718010324N55 , Date of registration: 27/05/2020, URL: https://en.irct.ir/user/trial/44986/view .
考虑到性功能的重要性,哺乳期妇女性功能障碍(尤其是萎缩性阴道炎引起的性交困难)的高发率,以及缺乏有效的干预措施,本研究旨在确定催产素(OXT)阴道凝胶对哺乳期妇女性功能(主要结局)、性满意度和抑郁(次要结局)的影响。
本随机三盲对照试验于 2020-21 年在伊朗大不里士市的健康中心招募了 64 名哺乳期妇女。参与者采用区组随机化方法等分为干预组和对照组。干预组每天给予 200IU 的 OXT 阴道凝胶,共 8 周,对照组给予安慰剂,方案相同。在基线和干预 8 周后,使用女性性功能指数(FSFI)、爱丁堡产后抑郁量表(EPDS)和女性性满意度量表(SSSW)的标准问卷对两组进行评估。采用协方差分析(ANCOVA)比较两组干预后平均总分的差异,调整基线值。
干预后,两组 FSFI 总分的平均差异无统计学意义(调整平均差异(AMD):1.14;95%置信区间(95%CI):-1.28 至 9.16;P=0.349)和性满意度(AMD:5.01;95%CI:-0.53 至 10.56;P=0.075)。然而,两组在性满足感的平均得分方面存在统计学差异(AMD:1.56;95%CI:0.29 至 2.83;P=0.017)和抑郁(AMD:-1.90;95%CI:-1.27 至 -2.54;P<0.001)。OXT 组有 1 名参与者和安慰剂组有 1 名参与者报告轻微子宫收缩,安慰剂组有 1 名参与者报告阴道烧灼感。
没有证据表明 OXT 凝胶能改善 FSFI,尽管与安慰剂组相比,OXT 能显著改善满足感方面的性满意度,并改善抑郁症状。然而,这需要在这方面进行更多的研究才能得出明确的结论。
伊朗临床试验注册中心(IRCT),编号:IRCT20120718010324N55,注册日期:2020 年 5 月 27 日,网址:https://en.irct.ir/user/trial/44986/view。