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临床试验/ACTRN12613001207707
ACTRN12613001207707已完成未知

Pilot Study for a trial in Human Papillomavirus (HPV) vaccinated and unvaccinated women presenting for cervical screening of 6 yearly HPV screening versus 3-yearly cytology screening to assess the feasibility via recruitment rates, cross sectional positivity rate and laboratory implementation.

Roche Molecular Systems Inc. and0 个研究点目标入组 5,001 人开始时间: 2013年11月4日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
5,001

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Open (masking not used)

入排标准

年龄范围
25 Years 至 64 Years(—)
性别
Female

入选标准

  • Australian female resident of Victoria
  • Aged 25-64
  • Attending for routine cervical screening at a participating health care practice

排除标准

  • Total hysterectomy (uterus and cervix)
  • Presence of symptoms for which cervical cancer must be excluded
  • Currently undergoing treatment for cervical pre-cancer, or cancer
  • Attending for follow-up of a prior cervical abnormality, including repeated test of cure procedures in which the woman has not yet been discharged back to routine screening
  • Known pregnancy

研究者

发起方
Roche Molecular Systems Inc. and

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