ISRCTN57612064已完成不适用
Efficacy trial of human papillomavirus (HPV) versus Pap testing for screening cervical cancer precursors: a randomised controlled trial
McGill University (Canada) - Research Grants Office0 个研究点目标入组 10,154 人开始时间: 2005年9月9日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 10,154
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
- •Current inclusion criteria as of 05/01/2010:
- •1. Women aged 30 to 69 years
- •2. Sought screening tests for cervical cancer in any of 30 family practice or gynaecology clinics in Montreal and St. John's, Canada
- •Initial inclusion criteria at time of registration:
- •1. Women aged between 30 and 69 years
- •2. Currently attending a colposcopy clinic for evaluation, treatment or follow up of a cervical lesion
排除标准
- •Current exclusion criteria as of 05/01/2010:
- •1. Currently being followed up for a cervical lesion
- •2. Lacked a cervix
- •3. Pregnant
- •4. Had a history of cervical cancer
- •5. Had undergone Pap testing in the previous year
- •6. Unable to provide consent were excluded (note that this is related also to the ability to understand French or English)
- •Initial exclusion criteria at time of registration:
- •1. Without a cervix
- •2. Pregnant
- •3. History of cervical cancer
- •4. Known human immunodeficiency virus (HIV) infection
- •5. Mentally incompetent
- •6. Unable to understand French or English
- •7. Refuse to provide an informed consent
研究者
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