ISRCTN22944015已完成不适用
Comparison of cervical SCREENing using visual inspection with acetic acid (VIA), to Swede score using GYNOCULAR in detecting cervical intraepithelial Neoplasia (CIN) lesions: a multicentre prospective randomized clinical trial
H&M Conscious Foundation (Sweden)0 个研究点目标入组 1,000 人开始时间: 2014年5月15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
- 1,000
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. Age between 25-65
- •2. No current significant vaginal bleeding
- •3. No current clinical signs of pelvic infection
- •4. No current clinical signs of acute cervicitis
- •5. More than one week since any last pelvic gynecological examination
- •6. Able to understand written and/or oral information
- •7. Mentally capable of providing informed consent
排除标准
- •1. Not fulfilling any of the inclusion criteria
- •2. Gross cervical lesions suggestive of invasion (cancer)
- •3. Pregnancy
- •4. Less than 3 months since last delivery or miscarriage
- •5. Lesions involving > 75% (subjective) of the cervix are excludd from same day outpatient treatment
- •6. Lesions with endocervical involvement > 2mm are excluded from cold coagulation
- •7. Bleeding disorders
- •8. Sensitivity to any of the drugs/materials used
研究者
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