ITMCTR1900002767尚未招募4 期
A randomized, blind, positive-controlled, multicenter study to evaluate the efficacy and safety of Compound Furong effervescent suppository in the treatment of bacterial vaginosis combined with aerobi
Beijing Tsinghua Changgeng Hospital0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 20 至 55（—）
- 性别
- Female
入选标准
- •1. Clinical diagnosis of Bacterial Vaginosis combined with aerobic vaginitis;
- •2. conforms to the syndrome differentiation standard of TCM dampness-heat bet syndrome;
- •3. Donders score >= 3, <=6;
- •4. Nugent score >= 7;
- •5. Aged >= 20, <= 55 years, sexual life history;
- •6. The patient is willing to participate voluntarily and to sign the informed consent.
排除标准
- •1. Combined with other vaginitis such as trichomoniasis vaginitis, vulvovaginal candidiasis, or suspected gonorrhea, herpes simplex virus infection caused by reproductive tract infection;
- •2. Patients with other serious gynecological diseases, such as gynecological malignant tumor and pelvic inflammatory disease;
- •3. Patients with serious primary diseases such as heart, brain, liver, kidney, blood system and endocrine system, among which ALT or AST over 2-fold of normal value or Scr over normal value.
- •4. Patients who received any oral or external drug treatment for this disease within one week before enrollment;
- •5. Pregnancy, breast feeding and the possible pregnancy during study;
- •6. Those who are known to be allergic to the components of experimental drugs;
- •7. Persons who have combined neurological or mental disorders and are unable to cooperate, and who suspect or have a history of alcohol or drug abuse;
- •8. Patient who is participating in other trials or has been participated in other trials in recent 1 months before screen;
- •9. Not suitable for this study judged by investigater.
研究者
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