EUCTR2008-007763-16-AT进行中（未招募）1 期
Topical Imiquimod in Treating Patients with Grade 2/3 Cervical Intraepithelial Neoplasia - ITIC (Imiquimod Therapy in Cervical Intraepithelial Neoplasia)-Trial
Medizinische Universität Wien, Univ.Klinik f.Frauenheilkunde,Abt. f.Gynäkologie und Gyn.Onkologie0 个研究点目标入组 60 人开始时间: 2009年1月26日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Caucasian women aged 18 years and older with proven HPV-associated CIN 2/3
- •Colposcopy with fully visible transformation zone and lesion
- •Safe Contraception
- •Signed Informed Consent
- •Negative urine pregnancy test
- •Able to communicate well with the investigator, to understand and comply with the requirements of the study
- •Signed the written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Women who are pregnant or lactating or become pregnant during the conduct of the study
- •Symptoms of a clinically relevant illness in the 3 weeks before the first study day
- •History of hypersensitivity to the trial drug or to drugs with a similar chemical structure
- •Participance in another clinical trial within 30 days
- •Immunosuppression (medication, illness)
- •HIV- or Hepatitis infection
研究者
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