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临床试验/NCT01416922
NCT01416922Unknown不适用

The oncoFISH Cervical Test for Detection of 3q26 Region Gain

Ikonisys, Inc.1 个研究点 分布在 1 个国家目标入组 1,100 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
不适用
入组人数
1,100
试验地点
1

研究概览

简要总结

The purpose of this study is to evaluate the use of the oncoFISH cervical test system in the management of women who have received an LSIL Pap report to determine whether the test can predict which women will progress to more serious cervical disease and which women do not have to be monitored as closely.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Women 21 years of age or greater with recent LSIL who are scheduled for colposcipal assessment.
  • Women with previous or current STD or HIV may be included
  • Women with previous LSIL history may be included.

排除标准

  • pregnant women,
  • women with vaginal intraepithelial lesions,
  • women on a chemotherapeutic agent,
  • women with previous or current cancer except for non-cervical squamous cell carcinoma

研究者

申办方类型
Industry

研究点 (1)

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