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临床试验/IRCT201702197511N3
IRCT201702197511N3招募中早期 1 期

The effect of vaginal product based on chamomile for treatment of women with dyspareunia

Tehran University of Medical Sciences0 个研究点目标入组 92 人开始时间: 待定最近更新:
适应症

试验速览

阶段
早期 1 期
状态
招募中
入组人数
92

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 49 years(—)
性别
Female

入选标准

  • Patients aged 18 to 49 years old married women with dyspareunia at least during the 3 last months; having intercourse at least once during a month; conscious informed consent; normal gynecological examination; using non-hormonal contraceptives. Exclusion criteria: use of hormonal drugs, anti-hypertensive and anti-depressant drugs over a month before beginning of the study; pregnancy; breast-feeding; Menopause.

排除标准

  • 未提供

研究者

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