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临床试验/ITMCTR2200006081
ITMCTR2200006081尚未招募1 期

Clinical Effect of Quyou Prescription in the Treatment of Persistent High-risk HPV Infection

Fujian Provincial Maternity and Children's Hospital0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 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

性别
Female

入选标准

  • (1) meet one of the three conditions:?tested positive for HPV16/18 and pathological tissue result of LSIL or below,cervical colposcopy biopsy of LSIL or below,and LSIL lesions less than two years;?tested negative for HPV16 or 18,but positive for other types of high-risk HPV,cytological evidence of ACUS or above,cervical colposcopy biopsy of LSIL or below,and LSIL lesions less than two years;?tested negative for HPV16 or 18,but positive for other types of high-risk HPV,cytological evidence of NILM;
  • (2) homotype HPV infection more than half a year;
  • (3) conforming to the standard of TCM syndrome of dampness and heat;
  • (4) women aged 25-65 with a history of sexual life and regular menstrual cycles;
  • (5) patients with normal liver and kidney function and no history of severe drug allergy;
  • (6) gave informed consent volunteering to participate in the study.

排除标准

  • (1) women who were not avoiding pregnancy,were pregnant, or were breastfeeding;
  • (2) those who had used other HPV drugs in the first 3 months of enrollment;
  • (3) patients participating in clinical trials of other drugs.;
  • (4) allergic constitution, such as allergic history of two or more drugs and food,or allergic to the ingredients of a given drug;
  • (5) patients with HSIL or above indicated by cervical biopsy under colposcopy.

研究者

发起方
Fujian Provincial Maternity and Children's Hospital

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