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临床试验/ISRCTN72259107
ISRCTN72259107已完成不适用

A comparison of the performance of the Gynocolar and stationary colposcope by the Swede score colposcopy system in women with abnormal cytology: a randomized cross-over trial

Gynius AB (Sweden)0 个研究点目标入组 125 人开始时间: 2014年1月30日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
125

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

性别
Female

入选标准

  • 1. Women with atypical cells of undetermined significance (ASC-US) or low-grade squamous intraepithelial lesion (LSIL) and high-risk human papillomavirus (HPV) and HR HPV positivity, or any high grade lesion (CIN II or more) regardless of HPV status, referred for colposcopy to the Department of Obstetrics and Gynecology, Danderyd Hospital, Stockholm, Sweden between June 2012 and June 2013
  • 2. Ability to understand written and oral information in Swedish
  • 3. Willingness to sign informed consent to take part in the study after oral and written information

排除标准

  • 1. Ongoing vaginal bleeding
  • 2. Any previous gynecological examinations within a week prior to the examination
  • 3. Pregnancy

研究者

发起方
Gynius AB (Sweden)

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