跳至主要内容
临床试验/NCT00182481
NCT00182481已完成不适用

Long Term Management of Asthma (LOMA) Study- How Useful is the Sputum Count Compared With the Usual Clincal Variables?

Hamilton Health Sciences Corporation2 个研究点 分布在 1 个国家目标入组 112 人开始时间: 1999年9月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
112
试验地点
2
主要终点
Relative risk reduction for the occurence of the first exacerbation and the length of time without exacerbation during Phase 2 of the study.

研究概览

简要总结

The purpose of this study was to determine whether the use of induced sputum cell counts could guide treatment of asthma more effectively than the use of symptoms and breathing tests. The main outcomes where the time to the first exacerbation and the number of exacerbations.

详细描述

Airway inflammation is an important component of asthma. It influences other components which include symptoms and airway functional (physiological) measurements. It is the primary target of treatment. However, it does not correlate closely with symptoms, need for symptomatic bronchodilator relief, or the physiological abnormalities. Furthermore, it can be of different types. As a result, physicians are poor at recognizing its presence or type. This is important because eosinophilic inflammation is responsive to corticosteroid while non-eosinophilic is not responsive.

The most comprehensive non-invasive or relatively non-invasive measurement of airway inflammation is by spontaneous or induced sputum cell counts. These are reliable, valid and responsive, the qualities of good measurements. They might therefore be clinically useful to guide individual treatment. In the present study we investigated this issue. We compared their use, in comparison with the use only of symptoms and spirometry, in preventing exacerbations of asthma. We chose prevention of exacerbations as the most important clinical outcome because these have the greatest impact on patient's quality of life, morbidity and healthcare utilization. The study comprised two Phases. In Phase 1, the minimum treatment to control sputum eosinophilia (as well as clinical criteria) in the Sputum Strategy, and clinical criteria in the Clinical Strategy, were established. In Phase 2, this minimum treatment was maintained and patients were seen every 3 momths and at exacerbations. The primary outcomes were the relative risk reduction for the occurrence of the first exacerbation and the length of time without exacerbation over 18-20 months in Phase 2 of the study.

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
Single

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • History of asthma for at least one year,confirmed objectively.
  • New or previously reviewed patients where the minimal treatment requirements have not been established within the last six months.

排除标准

  • Smokers or ex-smokers for less than 6 months with a smoking history of more than 10 pack years.
  • Other pulmonary co-morbidity (other than mild or moderate chronic airflow limitation).
  • Subjects having a co-existing illness that precludes them from the study.
  • Inability to give informed consent due to mental or legal reasons.
  • Pregnancy or lactation.
  • Known non-compliance with medications.

结局指标

主要结局

Relative risk reduction for the occurence of the first exacerbation and the length of time without exacerbation during Phase 2 of the study.

次要结局

  • Secondary outcomes were
  • The cellular type of exacerbation that was influenced,
  • The severity of asthma that was helped,
  • The dose of inhaled corticosteroid that was required,
  • Symptom control,
  • Quality of life,
  • FEV1
  • Methacholine PC20,
  • Cost effectiveness and cost benefit of sputum cell counts, Airway structural changes
  • Exhaled NO,
  • Skin bruising score.

研究者

申办方类型
Other

研究点 (2)

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