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临床试验/NCT06060691
NCT06060691已完成1 期

Randomized Controlled Trial Studying the Ameliorating Effects of Kaempferol Emulgel on Female Arousal Disorder and Sexual Dysfunction

Deraya University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年9月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
30
试验地点
1
主要终点
Female Sexual Function Index

研究概览

简要总结

The aim of this study is to evaluate the quality of sexual life of females with sexual interest or arousal disorder before and after accurate application of a formulated emulgel made from natural ingredients, including kaempferol as an API

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Women between the ages of 28 and 45
  • had regular periods and previous menstrual bleeding lasted between three and seven days

排除标准

  • sensitivity to drug of therapy,
  • autoimmune illness,
  • smoking or drinking,
  • liver disease,
  • irregular menstruation

研究组 & 干预措施

Kaempferol group

Experimental

Kaempferol gel received the vaginal gel containing antioxidant extract every day for seven days. Then, the treatment continued for two months, twice weekly

干预措施: Kaempferol (Drug)

Placebo group

Placebo Comparator

Plain formulation received the vaginal gel containing antioxidant extract every day for seven days. Then, the treatment continued for two months, twice weekly

干预措施: Kaempferol (Drug)

结局指标

主要结局

Female Sexual Function Index

时间窗: two months

The FSFI comprises 19 questions of sexual function in six independent areas consisting of desire, arousal, lubrication, orgasm, sexual satisfaction , pain from sex.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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