IRCT20230811059116N1尚未招募3 期
The effect of topical Imiquimod5% in treatment of high-grade cervical neoplasias (CIN2,3)
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 80
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
- 年龄范围
- 20 years 至 45 years(—)
- 性别
- Female
入选标准
- •Age 20-45 years old
- •Diagnosis of high-grade cervical neoplasia (CIN2,3)
- •Obtaining informed consent
排除标准
- •Cortone therapy
- •Suppressed immune system due to HIV or organ transplant
- •Prior treatment for HSI
研究者
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撤回
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不适用
Clinical and immunological effects of imiquimod and HPV-vaccination compared to imiquimod alone in female patients with Usual type VIN - Effects of HPV-vaccination and imiquimod in VIN patientsIn this trial, the efficacy of Gardasil combined with imiquimod in women with usual type Vulvar Intraepithelial Neoplasia is investigated.MedDRA version: 9.1Level: LLTClassification code 10047778Term: Vulvar cancer in situMedDRA version: 9.1Level: LLTClassification code 10066416Term: Vulvovaginal human papilloma virus infectionMedDRA version: 9.1Level: LLTClassification code 10046859Term: VaccinationMedDRA version: 9.1Level: LLTClassification code 10062059Term: Histology abnormalEUCTR2008-008251-42-NLErasmus MC
