EUCTR2008-005746-22-DE进行中(未招募)不适用
Multi-center, double blind, dose escalating study to compare the effects of 5 mg, 10mg and 20mg of Desloratadine in patients with acquired cold urticaria (ACU) - AECUDATT
Allergie-Centrum-Charite, Department of Dermatology, Charite - Universitätsmedizin Berlin0 个研究点目标入组 30 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
- 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
- •Informed consent signed and dated
- •Reliable method of contraception for both women of childbearing potential as well as man during the study and 3 months thereafter. A highly effective method of birth control is defined as those which result in a low failure rate (i.e. less than 1% per year) when used consistently and correctly such as implants, injectables, combined oral contraceptives, some IUDs, sexual abstinence or vasectomised partner
- •Outpatients with ACU for more than 6 weeks. Urticaria symptoms must comprise wheal and itch.
- •Age between 18 and 75 years.
- •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
- •Subjects who are inmates of psychiatric wards, prisons, or other state institutions. Existing or planned placement in an institution after ruling according to § 40 passage 1 number 4 AMG (Arzneimittelgesetz).
- •The presence of permanent severe diseases, especially those affecting the immune system, except urticaria and cold urticaria
- •The presence of permanent gastrointestinal condition which may influence the oral therapy (chronic diarrhoea diseases, congenital malformations or surgical mutilations of gastrointestinal tract)
- •History or presence of epilepsy, significant neurological disorders, cerebrovascular attacks or ischemia
- •History or presence of myocardial infarction or cardiac arrhythmia which requires drug therapy
- •Evidence of severe renal dysfunction
- •Evidence of significant hepatic disease (liver enzymes twice the upper reference value)
- •History of adverse reactions to DL
- •Presence of active cancer which requires chemotherapy or radiation therapy
- •Presence of alcohol abuse or drug addiction
- •Intake of oral corticosteroids within 14 days prior to screening visit
- •Use of depot corticosteroids or chronic systemic corticosteroids within 21 days prior to screening visit
- •Use of systemic immunosupressants/immunomodulators like ciclosporine A, dapsone, methotrexate, mycophenolate, chloroquine, and comparable drugs within 28 days prior to screening visit.
- •Pregnancy or breast-feeding
研究者
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