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临床试验/NCT00914654
NCT00914654Unknown4 期

Blood and Urinary Concentrations of Inhaled Formoterol in Asthmatic Subjects and Elite Athletes With Asthma

Bispebjerg Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2009年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
30
试验地点
1
主要终点
Serum and urine concentrations of formoterol

研究概览

简要总结

The purpose of the study is to assess the blood and urine concentrations of inhaled formoterol.

详细描述

The purpose of the study is to assess the serum and urine concentrations after inhalation of 18 microgram formoterol as one dose.

Furthermore to investigate the serum and urine concentrations of inhaled formoterol and evaluate the difference between three groups: healthy men, male asthmatic subjects and male elite athletes with asthma.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Physician-diagnosed asthma with positive reversibility or challenge test.
  • Informed consent.
  • Age between 18-45 years.
  • Sex: male.
  • Asthma classified as mild to moderate according to GINA guidelines.
  • Used beta-2-agonist in minimum 12 months.

排除标准

  • Smokers or ex-smokers with a smoking history of 10 pack years or more.
  • Respiratory tract infections within the last 2 weeks prior to study day.
  • Subjects with other chronic diseases than asthma and allergy.
  • Allergy towards the study medicine.
  • Use of beta-2-agonist 10 days prior to study day.

研究组 & 干预措施

Healthty

Other

10 healthy men

干预措施: inhaled formoterol (Drug)

Asthmatics

Other

10 male asthmatic subjects

干预措施: inhaled formoterol (Drug)

Elite asthmatics

Other

10 male elite athletes with asthma

干预措施: inhaled formoterol (Drug)

结局指标

主要结局

Serum and urine concentrations of formoterol

时间窗: baseline, 4, 8, and 12 hours after medicine administration

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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