An open, single center, clinical investigation to evaluate the efficacy and safety of a non-hormonal vaginal moisturizer for the symptomatic treatment of vulvovaginal atrophy in postmenopausal woman.

IF 2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Gynecological Endocrinology Pub Date : 2025-12-01 Epub Date: 2025-05-05 DOI:10.1080/09513590.2025.2500480
Manuel Sánchez-Prieto, Nicolás Mendoza, Peter Chedraui, Félix Lugo-Salcedo, Aida Serra-Ribas, Sonia Aladrén-Pérez, Javier Bustos-Santafé, Rafael Sánchez-Borrego
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引用次数: 0

Abstract

Objective: To evaluate the efficacy and safety of a non-hormonal vaginal moisturizer in alleviating the clinical symptoms of vulvovaginal atrophy (VVA).

Methods: This was an observational, single center, open label study in which the investigational product was applied to postmenopausal women (n = 36) with VVA symptoms three times per week for a period of 12 weeks. Patient's perception of vaginal discomfort, sexual function improvement assessed with the Female Sexual Function Index (FSFI), quality of life evaluated with the Cervantes-SF scale, and subject's satisfaction with the treatment were evaluated after 4 and 12 weeks of product use. In addition, vaginal health was evaluated with the Vaginal Health Index (VHI) score and the vaginal pH.

Results: A statistically significant decrease was observed in the severity of the most bothersome symptoms from moderate at baseline (mean 2.47 ± 0.55) to mild after 4 weeks (mean 1.33 ± 0.58) and 12 weeks (mean 1.32 ± 0.74, p < 0.0001). VHI scores significantly improved after 4 and 12 weeks compared to baseline (from 11.70 to 16.36 at 4 weeks and 17.34 at 12 weeks, both p < 0.0001). Vaginal pH decreased significantly from a mean pH of 6.27 ± 0.46 at baseline to 5.77 ± 0.59 at 4 weeks and 5.56 ± 0.60 at 12 weeks of treatment (p < 0.0001). Total FSFI scores significantly increased, indicating improvement of sexual function, after 4 and then after 12 weeks of product use (Baseline score 20.16 compared to 24.27 at 4 and 23.94 at 12 weeks, both p < 0.0001). Quality of life improved (decrease of total Cervantes-SF scores) after 12 weeks of product use as compared to baseline (Baseline 32.09 vs 26.45, p = 0.0004). At 12 weeks, a 97.5% reported overall satisfaction with the product and no adverse events related to the product were reported.

Conclusion: Through limited size study, the proposed non-hormonal vaginal moisturizer demonstrated being effective and safe for the management of VVA symptoms in postmenopausal women, offering significant improvements in symptom severity, vaginal health, sexual function, and quality of life. There is a need for further research with a larger sample and comparison with other similar products.

一项开放的、单中心的临床研究,评估非激素阴道保湿剂对症治疗绝经后妇女外阴阴道萎缩的疗效和安全性。
目的:评价一种非激素阴道保湿剂缓解外阴阴道萎缩(VVA)临床症状的疗效和安全性。方法:这是一项观察性、单中心、开放标签研究,研究产品应用于有VVA症状的绝经后妇女(n = 36),每周3次,持续12周。在使用4周和12周后,分别评估患者阴道不适的感觉、女性性功能指数(FSFI)评估的性功能改善情况、塞万提斯- sf量表评估的生活质量以及受试者对治疗的满意度。结果:在4周(平均1.33±0.58)和12周(平均1.32±0.74,p p p p = 0.0004)后,最令人烦恼的症状的严重程度从基线时的中度(平均2.47±0.55)降低到轻度(平均1.47±0.74),具有统计学意义。在12周时,97.5%的人报告了对产品的总体满意度,没有报告与产品相关的不良事件。结论:通过有限规模的研究,所提出的非激素阴道保湿剂对绝经后妇女VVA症状的治疗是有效和安全的,在症状严重程度、阴道健康、性功能和生活质量方面有显著改善。有必要进行更大样本的进一步研究,并与其他类似产品进行比较。
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来源期刊
Gynecological Endocrinology
Gynecological Endocrinology 医学-妇产科学
CiteScore
4.40
自引率
5.00%
发文量
137
审稿时长
3-6 weeks
期刊介绍: Gynecological Endocrinology , the official journal of the International Society of Gynecological Endocrinology, covers all the experimental, clinical and therapeutic aspects of this ever more important discipline. It includes, amongst others, papers relating to the control and function of the different endocrine glands in females, the effects of reproductive events on the endocrine system, and the consequences of endocrine disorders on reproduction
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