DRKS00012471招募中未知
Characterization of the extent, the time course and the underlying pathomechanism of the elevated skin reactivity of chronic urticaria patients in comparison with healthy test subjects. - Skinsensitivity in chronic urticaria - SkisiC
Charite-Universitätsmedizin Berlin, Klinik für Dermatologie und Allergologie0 个研究点目标入组 95 人开始时间: 2017年5月31日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 95
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 100 Years（—）
- 性别
- All
入选标准
- •Adults (18 years or older)
- •Able to read, understand and willing to sign the informed consent form and abide with study procedures
- •Willing, committed and able to complete all study-related procedures
- •Arm1: Diagnosis of urticaria for more than 6 weeks
- •Patients may have additional concomitant disease, but only one dominant skin disease.
- •No participation in other clinical trials 4 weeks before in this study
排除标准
- •Concurrent/ongoing treatment with immunosuppressives (e.g. cyclosporine, methotrexate, dapsone, systemic Corticosteroids or others) within 4 weeks or 5 half lives prior to study entry whichever is longer
- •Concurrent/ongoing treatment with Omomalizumab within 3 months prior to study entry
- •Prior or concurrent treatment with antihistamines within the last 5 days.
- •Significant medical condition rendering the patient immunocompromised or not suitable for a clinical trial
- •Lactating females or pregnant females
- •Any medical condition which, in the opinion of the Investigator, would interfere with participation in the study or place the subject at risk
- •Intake of leukotriene antagonists within 7 days prior to study entry
- •History of hypersensitivity/allergy to local anesthetics
研究者
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