EUCTR2004-002823-42-IT进行中(未招募)不适用
A multicentre, double-blind, parallel, randomized, placebo-controlled study Evaluation of the efficacy and safety of Levocetirizine 5 mg and Desloratadine 5 mg administered orally as capsules once daily, in the morning, over 2 weeks in patients suffering from Allergic Rhinitis AR
CB PHARMA0 个研究点目标入组 729 人开始时间: 2006年1月5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
- 729
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
- •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
- 未提供
研究者
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A multicentre, double-blind, parallel, randomized, placebo-controlled study :Evaluation of the efficacy and safety of Levocetirizine 5 mg and Desloratadine 5 mgadministered orally as capsules once daily, in the morning, over 2 weeks in patientssuffering from Seasonal Allergic Rhinitis (SAR) due to grass polleAllergic Rhinitis (AR)MedDRA version: 7.1Level: LLTClassification code 10001723EUCTR2004-002823-42-DECB S.A. Pharma Sector729
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