EUCTR2005-006133-32-DE进行中（未招募）不适用
An exploratory phase IV, randomised, double-blind, placebo controlled crossover study to assess and compare the effects of 5 mg vs. 20 mg Desloratadine on the development of experimentally induced urticaria lesions - AUDAC
Allergie-Centrum-Charité0 个研究点目标入组 30 人开始时间: 2006年6月28日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 30
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
- All
入选标准
- •ACU patients aged 18-70 years, signed written consent, no systemic corticosteroid or other immunosuppressive therapy, no permanent severe diseases
- •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
- •The presence of permanent severe diseases, especially those affecting the immune system, except ACU, History of adverse reactions to Desloratadine, Intake of corticoids with the last 14 days, History or presence of alcohol abuse or drug addiction, Pregnancy or breast-feeding
研究者
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