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临床试验/NCT06067100
NCT06067100招募中不适用

Physiological Response to U-LABA/ICS With Emphasis on Exercise Performance, Indacaterol

Morten Hostrup, PhD1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年1月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
30
试验地点
1
主要终点
Power output during sprint testing

研究概览

简要总结

The purpose of the project is to investigate exercise performance in humans following bronchodilation induced by acute inhalation of beta2-agonist indacaterol + mometasonefuroate

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 39 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-39
  • Physically active > 5 h weekly
  • Maximal oxygen consumption classified as high or very high

排除标准

  • Diagnosed with severe asthma and been in treatment with long-acting beta2-agonist/corticosteroid
  • ECG abnormality
  • ACQ score > 1.5
  • Severe bronchial hyperreactivity as determined by mannitol test
  • FEV1/FVC ratio < 0.7 determined with spirometry
  • Chronic illness determined to be a potential risk for participant during study
  • In chronic treatment with medication that may interfere with study results
  • Pregnancy
  • Blood donation during the past 3 months

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

Indacaterol + mometasonefluroate

Experimental

干预措施: Indacaterol and Mometasonefluroate (low dose) (Drug)

Indacaterol + mometasonefluroate

Experimental

干预措施: Indacaterol and Mometasonefluroate (high dose) (Drug)

结局指标

主要结局

Power output during sprint testing

时间窗: Through study completion, an average of 3 weeks

Power output measured in Watts during a sprint on a bike ergometer

次要结局

  • Power output during time trial(Through study completion, an average of 3 weeks)
  • Forced Expiratory Volume in 1 second (FEV1)(Through study completion, an average of 3 weeks)
  • Quadriceps strength(Through study completion, an average of 3 weeks)
  • Respiratory muscle function(Through study completion, an average of 3 weeks)

研究者

发起方
Morten Hostrup, PhD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Morten Hostrup, PhD

Associate Professor

University of Copenhagen

研究点 (1)

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