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临床试验/IRCT2016062528613N1
IRCT2016062528613N1已完成1 期

Assessment effect of suppository of a drug based on Percian medicine on bacterial vaginosis

Tehran University of Medical Science0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
120

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
15 years 至 50 years(—)
性别
Female

入选标准

  • Outpatient women aged 18- 50 years with symptoms such as burning and itching refer and amsel criteria for bacterial vaginosis is positive for them; that Both treatments (chemical or herbal) do not use;They do not suffer from organic diseases such as cancer or other malignancies of the uterus or ovaries or Patients with chronic diseases. Exclusion criteria: Patients who use other antibiotics during the study; Patients who are experiencing possible side effect; Patients who have other medical interventions needed;This group of patients who have a severe form of the disease and other therapies and may require hospitalization have been included; Patients who request personal decision to withdraw from the study; Patients with immunosuppressive disorders; people with HIV; Patients with other infections such as genital herpes or trichomoniasis or fungal or gonorrhea at the same time with bacterial vaginosis; People who take other medication Such as the use of immunosuppressive drug or consumers of anti-inflammatory;consumers of showers vaginal and vaginal acidifying agents

排除标准

  • 未提供

研究者

发起方
Tehran University of Medical Science

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