跳至主要内容
临床试验/NCT03923985
NCT03923985已完成不适用

Clinical Trial to Evaluate the Effect of an Oral Probiotic (Food Supplement) Containing Lactobacillus Crispatus on the Vaginal Flora

Instituto Palacios2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年3月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Changes in the number of Lactobacillus Crispatus on the vaginal flora

研究概览

简要总结

Clinical trial to evaluate the effect of a probiotic containing Lactobacillus Crispatus on the vaginal flora

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Healthy women between 18 and 45 years old
  • Women without current symptoms of vaginal infection
  • Negative bacteriological and clinical examination

排除标准

  • Women with vaginal infection
  • Women with undiagnosed vaginal bleeding
  • Patients with endometrial hyperplasia
  • Suspicion of neoplasia or active neoplasia
  • Women with intolerance, allergy or hypersensitivity to the components of the probiotic
  • Women with immunosuppressive disorders or with HIV
  • Women who are currently using probiotics by any route of administration
  • Women who are using some treatment for vaginal sepsis
  • Chronic decompensated noncommunicable diseases (diabetes mellitus, heart disease ...)
  • Pregnant women or those with precocious menopause

结局指标

主要结局

Changes in the number of Lactobacillus Crispatus on the vaginal flora

时间窗: Screening, month 2

Analysis of vaginal lactobacilli.

次要结局

  • Changes in vaginal PH(Screening, month 2)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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