NCT00623701已完成3 期
A Multicentre, Multinational, Placebo-controlled, Double-blind, Randomized Study to Evaluate Efficacy and Safety of a Perennial, Sublingual, Specific Immunotherapy in Patients With Rhinoconjunctivitis With/Without Controlled Asthma Caused by Grass Pollen
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 126
- 试验地点
- 2
- 主要终点
- Symptom and Medication Score
研究概览
简要总结
Efficacy and Safety from a high-dosed sublingual grass pollen preparation
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Allergic rhinoconjunctivitis attributable to grass pollen
- •Positive SPT
- •Positive EAST
- •Positive provocation Test
排除标准
- •Serious chronic disease
- •other perennial allergies
结局指标
主要结局
Symptom and Medication Score
时间窗: Grass pollen season 2009
次要结局
未报告次要终点
研究者
研究点 (2)
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