DRKS00004312已完成2 期
Efficacy of gencydo nasal spray on early nasal response after allergen exposition in patients with grass pollen allergy, a randomized, placebo controlled cross over study
iversitätsklinikum Freiburg, Leitender ärztlicher Direktor0 个研究点目标入组 41 人开始时间: 2012年10月29日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 41
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
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 50 Years（—）
- 性别
- All
入选标准
- •men and women aged between 18 - 50 years
- •-symptoms of grass polen allergy for at least 2 years (sneezing, itching of nose, running nose, tears)
- •-proof of allergy through prick test
- •-signed consent
排除标准
- •Chronic serious illness (i.e. diabetes mellitus type I, chronic polyarthritis, tumors, heart insufficiency, HIV-Infection)
- •Asthma bronchiale with continuous therapy with inhalative or systemic steroides
- •Hypersensitivity against compounds of Gencydo (quince, lemon)
- •Treatment with Gencydo Nasal Spray within the last month before inclusion into the study
- •Therapy with antihistamines, Cromoglycine acid, steroides or other antiallergic medication with 2 weeks before inclusion into the study
- •anamnestic alcohol abuse >30g/d or iv. drug abuse
- •pregnancy or breat feeding
- •simultaneous participation in another clinical study within 3 months before inclusion into the study
- •acute infection of airways or allergic reaction with distant symptoms
研究者
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