跳至主要内容
临床试验/NCT00273026
NCT00273026终止4 期

An Open-label, Multi-centre, Randomized, Parallel Group Clinical Effectiveness Study to Determine the Level of Asthma Control in Adolescent and Adult Patients With ADVAIR Versus Usual Care for 24 Weeks.

GlaxoSmithKline133 个研究点 分布在 1 个国家目标入组 680 人开始时间: 2004年11月8日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
680
试验地点
133
主要终点
Percentage of patients achieving well-controlled asthma at the end of the treatment period.

研究概览

简要总结

This study will compare patients treated with a marketed medication and those who continue with their usual care to assess the proportion of patients achieving well controlled asthma after 24 weeks.

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
None

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • documented clinical history of asthma and receiving regular maintenance therapy.

排除标准

  • Using oral/parenteral or depot corticosteroids within 12 weeks of visit
  • History of heavy smoking or substance abuse.
  • Females who are pregnant or lactating.
  • Required emergency room treatment for their asthma 12 weeks prior to Visit
  • Serious, uncontrolled, systemic disease that may make study participation unsafe or inappropriate in the opinion of the physician.
  • Other medical criteria will be evaluated at the screening visit.

结局指标

主要结局

Percentage of patients achieving well-controlled asthma at the end of the treatment period.

次要结局

  • Percentage of patients achieving total asthma control as defined by the Canadian Asthma consensus guidelines at the end of the treatment period.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (133)

Loading locations...

相似试验