Time-Effect of Montelukast on Protection Against Exercise-Induced Bronchoconstriction
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 69
- 试验地点
- 1
- 主要终点
- maximal percentage fall in FEV1 after exercise test from the baseline value
研究概览
简要总结
The aim of this study is to verify MNT time of onset of protection against EIB in asthmatic children by evaluating different time intervals between dosing and challenge, after a single-dose and after three days of once a day MNT administration.
详细描述
Within few days after a baseline exercise challenge, children was randomized to a double blind, placebo-controlled, three day doses, crossover study design. In practice each eligible patient was randomized by a computer-generated schedule to receive in sequence double-blind treatments with placebo or MNT (5 mg). Patients in sequence 1 received MNT, then crossed over to matching placebo; vice versa the case was for patients in sequence 2. Placebo and active treatments were separated by a 7-10 day wash-out period. Each child was assigned to one out of seven groups in order to perform the exercise challenge at different time intervals from drug administration which occurred always at 8.00 A.M. On day one the challenge was performed in the different groups 1, 2, 3, 4, 5, 6, and 8 hours after drug administration, respectively. Then treatment was continued as a single day dose for three consecutive days and a third challenge was then performed at the same time of the day.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 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
- 否
入选标准
- •children with exercise-induced asthma
排除标准
- •viral infections
- •montelukast treatment
研究组 & 干预措施
Montelukast
capsules prepared in blindness
干预措施: Montelukast (Drug)
Placebo
matched placebo
干预措施: Placebo (Drug)
结局指标
主要结局
maximal percentage fall in FEV1 after exercise test from the baseline value
时间窗: at the first and at the third day of single day drug administration
次要结局
- clinical protection(at the first and at the third day of single day drug administration)
