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临床试验/NCT00289874
NCT00289874已完成3 期

A Multicenter, Double-Blind, Placebo Controlled, Randomized, Parallel-Group Study to Evaluate the Clinical Effect of Oral Montelukast Versus Placebo in Persistent Asthma Which is Also Active During Allergy Seasons in Pediatric Patients With Seasonal Aeroallergen Sensitivity

Organon and Co0 个研究点目标入组 421 人开始时间: 2006年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
421
主要终点
Percent Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1) at Week 3

研究概览

简要总结

This is a 3-week study to evaluate FEV1 following treatment with drugs in persistent asthma which is also active during allergy seasons in pediatric patients with seasonal aeroallergen sensitivity.

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
6 Years 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Male and female patients, ages 6 to 14 years, with persistent asthma that is also active during allergy season
  • Patients must demonstrate positive skin prick tests to seasonally relevant geographic aeroallergens

排除标准

  • Patient cannot have any other acute or chronic pulmonary disorder

研究组 & 干预措施

1

Experimental

montelukast

干预措施: montelukast sodium (Drug)

结局指标

主要结局

Percent Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1) at Week 3

时间窗: Baseline and week 3

Percent change from baseline in FEV1, a measure of airway function, at Week 3

次要结局

  • Percent Change From Baseline in Mean Daily "as Needed" β-agonist Use Over the 3-week Treatment Period(Baseline and Week 3)

研究者

申办方类型
Industry
责任方
Sponsor

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