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临床试验/NCT07038070
NCT07038070撤回不适用

A Randomized Controlled Trial Comparing the Efficacy of Topical Vaginal Estrogen Versus Topical Vaginal Estrogen Plus Via, a Hyaluronic Acid-Based Vaginal Moisturizer, in the Treatment of Genitourinary Syndrome of Menopause

NYU Langone Health2 个研究点 分布在 1 个国家目标入组 196 人开始时间: 2025年7月1日最近更新:
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
入组人数
196
试验地点
2
主要终点
Percent change in vulvovaginal symptom questionnaire (VSQ) score

研究概览

简要总结

This study aims to evaluate whether the administration of vaginal estrogen along with Via, a hyaluronic acid-based vaginal moisturizer, offers superior relief from symptoms of genitourinary syndrome of menopause (GSM) in the urogynecologic patient population, compared to administration of vaginal estrogen alone.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
45 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Postmenopausal (last menstrual period at least 12 months ago).
  • Aged 45 years or older and have symptoms of Genitourinary Syndrome of Menopause (GSM).
  • Have never tried vaginal estrogen therapy, or have tried vaginal estrogen therapy, but have not used vaginal estrogen and/or hyaluronic acid products for management of GSM symptoms within the last 3 months.
  • Capable of signing informed consent.
  • Capable and willing to follow all study-relation visits.

排除标准

  • Subjects currently diagnosed with or undergoing treatment for hormone-sensitive disease (e.g. breast cancer)
  • Subjects currently using systemic hormone replacement therapy
  • Subjects currently using estrogen hormonal therapies or hormone modulators (aromatase inhibitors or selective estrogen receptor modulators)

研究组 & 干预措施

Vaginal Estrogen Alone

Active Comparator

Participants will administer vaginal estrogen tablets nightly for 2 weeks, then twice weekly for 14 weeks.

干预措施: Vaginal estrogen tablet (Drug)

Vaginal Estrogen + Hyaluronic acid (HLA)

Experimental

Participants will administer vaginal estrogen tablets nightly for 2 weeks, then twice weekly for 14 weeks. Participants will concomitantly apply Via (Hyaluronic acid) nightly for 16 weeks.

干预措施: Vaginal estrogen tablet (Drug)

Vaginal Estrogen + Hyaluronic acid (HLA)

Experimental

Participants will administer vaginal estrogen tablets nightly for 2 weeks, then twice weekly for 14 weeks. Participants will concomitantly apply Via (Hyaluronic acid) nightly for 16 weeks.

干预措施: Via Solv Wellness (Hyaluronic Acid Therapy) (Device)

结局指标

主要结局

Percent change in vulvovaginal symptom questionnaire (VSQ) score

时间窗: Baseline, Week 16

The VSQ is a 21-item survey designed to measure vaginal symptoms, emotions, life impact due to vulvovaginal symptoms, and sexual impact of vulvovaginal symptoms. The scores range from 0 - 20 with the higher score meaning greater impact from vulvovaginal symptoms.

次要结局

  • Percent change in vaginal pH(Baseline, Week 16)
  • Change in vaginal maturation index (VMI)(Baseline, Week 16)
  • Number of adverse events related to treatment(Week 16)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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