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临床试验/NCT00259779
NCT00259779已完成3 期

A Randomised, Double Blind, Double Dummy, Multicentre Phase III Study Comparing the Efficacy of Budesonide/Formoterol (Symbicort® Forte Turbuhaler®) and Oral Prednisolone + Formoterol (Oxis® Turbuhaler) During Two Weeks, in COPD Patients With an Acute Exacerbation, Followed by Twelve Weeks Open Follow up Period With Budesonide/Formoterol (Symbicort Forte Turbuhaler)

AstraZeneca37 个研究点 分布在 5 个国家目标入组 120 人开始时间: 2005年9月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
AstraZeneca
入组人数
120
试验地点
37
主要终点
Forced Expiratory Volume in one second (FEV1)

研究概览

简要总结

To assess if Symbicort forte Turbuhaler (during two weeks) is as effective as an oral course of prednisolone + Oxis Turbuhaler (during two weeks) for the treatment of an acute exacerbation of Chronic Obstructive Pulmonary Disease (COPD).

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
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with chronic obstructive pulmonary disease and an acute exacerbation
  • After the acute treatment a simple pulmonary function test shows a value of 30%-60% of the predicted normal value.
  • Patients, who, based on the clinical examination after the initial acute treatment, are candidates for a course of oral steroids for the treatment of acute symptoms due to chronic obstructive pulmonary disease

排除标准

  • Diagnosis/history of asthma
  • Oxygen uptake (saturation) is <92% after the initial acute treatment
  • A requirement for regular use of oxygen therapy
  • Regular treatment with any inhaled steroid >1 000 µg/day at study entry
  • Additional inclusion and exclusion criteria will be evaluated by the investigator

结局指标

主要结局

Forced Expiratory Volume in one second (FEV1)

次要结局

  • Number of patients with treatment failures
  • Time to first exacerbation
  • Number of patients developing an exacerbation
  • Diary cards
  • Quality of Life
  • - Adverse Events (AEs)
  • Serious Adverse Events (SAEs) and Discontinuations due to AEs
  • Variables will be assessed before and over the 2+12 weeks treatment period

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (37)

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