NCT01942005已完成不适用
EVER/TMC Mutation as Marker of the Risk of Cutaneous Carcinoma in Immunosuppressed Patients,Especially Patients After Organ Transplantation and Patients With HIV Infection
Andreas Arnold1 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2010年1月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 144
- 试验地点
- 1
- 主要终点
- Detection of mutation / specific polymorphism of the EVER/TMC6 and/or EVER/TMC8 gen.
研究概览
简要总结
Detection of mutation / specific polymorphism of the EVER/TMC6 and/or EVER/TMC8 gen.
详细描述
correlation between possibly detected mutation/specific polymorphism and kind and number of neoplasm, age of patients, UV burden, duration and kind of immunosuppression.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •patients in an immunosuppressive condition either by immunosuppressants or by HIV infection
排除标准
- •written informed consent not given
结局指标
主要结局
Detection of mutation / specific polymorphism of the EVER/TMC6 and/or EVER/TMC8 gen.
时间窗: 7 years
次要结局
- correlation between possibly detected mutation/specific polymorphism of the EVER/TMC6 and/or EVER/TMC8 gen and a composite of kind and number of neoplasm, age of patients, UV burden, duration and kind of immunosuppression.(7 years)
研究者
Andreas Arnold
Dr. med. Andreas Arnold, senior physician
University Hospital, Basel, Switzerland
研究点 (1)
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