跳至主要内容
临床试验/NCT01634152
NCT01634152已完成3 期

A Randomised, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate Efficacy and Safety of Tiotropium Inhalation Solution (2.5 mcg and 5 mcg) Delivered Via Respimat® Inhaler Once Daily in the Evening Over 12 Weeks as add-on Controller Therapy on Top of Usual Care in Children (6 to 11 Years Old) With Severe Persistent Asthma

Boehringer Ingelheim94 个研究点 分布在 10 个国家目标入组 401 人开始时间: 2012年7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
401
试验地点
94
主要终点
FEV1 Peak(0-3h) Change From Baseline

研究概览

简要总结

The overall purpose of the trial is to evaluate efficacy and safety of tiotropium inhalation solution (2.5 mcg and 5 mcg) delivered via Respimat® inhaler once daily in the evening over 12 weeks, compared to placebo, as add-on controller therapy on top of usual care in children (6 to 11 years old) with severe persistent asthma.

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

入排标准

年龄范围
6 Years 至 11 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Placebo QD

Placebo Comparator

干预措施: Placebo (Drug)

Tiotropium low dose QD

Experimental

干预措施: Tiotropium low dose mcg (Drug)

Tiotropium medium dose QD

Experimental

干预措施: Tiotropium high dose (Drug)

结局指标

主要结局

FEV1 Peak(0-3h) Change From Baseline

时间窗: Baseline and 12 weeks

Change from baseline in peak forced expiratory volume in 1 second within the first 3 hours post dosing (FEV1 peak(0-3h)) measured at week 12. Measured values presented are actually adjusted means.

次要结局

  • Peak Expiratory Flow (PEF) a.m. Change From Baseline(Baseline and 12 weeks)
  • Trough FEV1 Change From Baseline(Baseline and 12 weeks)
  • FVC Peak(0-3h) Change From Baseline(Baseline and 12 weeks)
  • Trough FVC Change From Baseline(Baseline and 12 weeks)
  • FEV1 AUC (0-3h) Change From Baseline(Baseline and 10 mins before drug administration and 30 mins, 1 hour (h), 2h, 3h after drug administration at 12 weeks)
  • FVC AUC (0-3h) Change From Baseline(Baseline and 10 mins before drug administration and 30 mins, 1 hour (h), 2h, 3h after drug administration at 12 weeks)
  • FEV1 Change From Baseline at Each Individual Timepoint(Baseline and 10 mins before drug administration and 30 mins, 1 hour (h), 2h, 3h after drug administration at 12 weeks)
  • FVC Change From Baseline at Each Individual Timepoint(Baseline and 10 mins before drug administration and 30 mins, 1 hour (h), 2h, 3h after drug administration at 12 weeks)
  • Control of Asthma as Assessed by ACQ-IA Total Score(Baseline and 12 weeks)
  • ACQ-IA Total Score Responders(12 weeks)
  • Use of PRN Rescue Medication Per Day(Baseline and 12 weeks)
  • Use of PRN Rescue Medication During the Daytime(Baseline and 12 weeks)
  • Use of PRN Rescue Medication During the Night-time(Baseline and 12 weeks)
  • Peak Expiratory Flow (PEF) p.m. Change From Baseline(Baseline and 12 weeks)
  • Peak Expiratory Flow (PEF) Variability Change From Baseline(Baseline and 12 weeks)
  • FEV1 a.m. Change From Baseline(Baseline and 12 weeks)
  • FEV1 p.m. Change From Baseline(Baseline and 12 weeks)
  • Change From Baseline in Nighttime Awakenings(Baseline and 12 weeks)
  • Change From Baseline in Morning Asthma Symptoms(Baseline and 12 weeks)
  • Change From Baseline in Daytime Asthma Symptoms(Baseline and 12 weeks)
  • Change From Baseline in Daytime Activity Limitations(Baseline and 12 weeks)
  • Change From Baseline in Daytime Experiences of Shortness of Breath(Baseline and 12 weeks)
  • Change From Baseline in Daytime Experiences of Wheeze or Cough(Baseline and 12 weeks)
  • Change From Baseline in Asthma Symptom-free Days(Baseline and 12 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (94)

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