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临床试验/NCT01491802
NCT01491802已完成3 期

A 4-week Randomized, Double-blind, Crossover Study to Assess the Effect of a New LABA/LAMA Combination Versus LAMA Alone on Exertional Dyspnea, Exercise Endurance and Neuromechanical Coupling in Patients With GOLD Stage II COPD

Queen's University1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
17
试验地点
1
主要终点
Exertional Dyspnea Intensity at Isotime Exercise.

研究概览

简要总结

Preliminary information from our laboratory indicated that even patients with milder chronic obstructive pulmonary disease (COPD) can have significant physiological derangements which become more pronounced during exercise, leading to intolerable dyspnea at lower levels of ventilation than in health. This study will explore pathophysiological mechanisms of dyspnea and activity limitation in GOLD stage II COPD and will determine if there is a sound physiological rationale for the use of dual long-acting beta2-agonist (LABA)/long-acting muscarinic antagonist (LAMA) therapy (GSK573719/ GW642444 Inhalation Powder) versus LAMA alone (GSK573719) as treatment for dyspnea and exercise intolerance in this subpopulation. Objectives of this study are to determine if: 1) neuromechanical uncoupling of the respiratory system contributes to exertional dyspnea in milder COPD, and 2) treatment with LABA/LAMA improves dyspnea and exercise endurance compared with LAMA by improving neuromechanical coupling. The investigators hypothesize that: 1) dyspnea is related to excessive dynamic lung hyperinflation, tidal volume restriction and increased ratio of central respiratory neural drive to tidal volume displacement, a measure of neuromechanical uncoupling of the respiratory system, and 2) LABA/LAMA will improve dyspnea and exercise endurance, which will be explained by partial reversal of the above mechanical abnormalities. The investigators will conduct a randomized, double-blind crossover study and compare the effects of once-daily LABA/LAMA over 4-weeks with LAMA on dyspnea, exercise endurance and ventilatory mechanics in GOLD stage II COPD.

研究设计

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

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

  • Stable moderate COPD
  • Post-bronchodilator FEV1/FVC<0.7 and 50%≤FEV1<80% predicted
  • Baseline Dyspnea Index ≤ 9 and MRC dyspnea scale >2
  • Cigarette smoking history at least 20 pack-years

排除标准

  • Presence of a significant disease other than COPD that could contribute to dyspnea and exercise limitation
  • Important contraindications to clinical exercise testing
  • Use of daytime oxygen
  • History of asthma

研究组 & 干预措施

LAMA alone, then LAMA/LABA combination

Experimental

Participants will first receive an inhaled long-acting muscarinic antagonist (LAMA) once daily for 4 weeks. After a 2 week washout period, they will then receive the fixed-dose combination product [LAMA plus long-acting beta2-agonist (LABA)] once daily for 4 weeks.

干预措施: LAMA/LABA (Drug)

LAMA alone, then LAMA/LABA combination

Experimental

Participants will first receive an inhaled long-acting muscarinic antagonist (LAMA) once daily for 4 weeks. After a 2 week washout period, they will then receive the fixed-dose combination product [LAMA plus long-acting beta2-agonist (LABA)] once daily for 4 weeks.

干预措施: LAMA (Drug)

LABA/LAMA combination, then LAMA alone

Experimental

Participants will first receive a long-acting muscarinic antagonist (LAMA) plus long-acting beta2-agonist (LABA) combination product once daily for 4 weeks. After a 2 week washout period, they will then receive the LAMA single product once daily for 4 weeks.

干预措施: LAMA/LABA (Drug)

LABA/LAMA combination, then LAMA alone

Experimental

Participants will first receive a long-acting muscarinic antagonist (LAMA) plus long-acting beta2-agonist (LABA) combination product once daily for 4 weeks. After a 2 week washout period, they will then receive the LAMA single product once daily for 4 weeks.

干预措施: LAMA (Drug)

结局指标

主要结局

Exertional Dyspnea Intensity at Isotime Exercise.

时间窗: 4 weeks

Intensity of dyspnea (defined as breathing discomfort) at a standardized time (isotime) during constant work rate exercise tests as measured by the modified 10-point Borg scale. A rating of 0 represents no dyspnea up to a maximum of 10: a smaller rating is therefore an improvement. Isotime was defined as the highest exercise time in minutes completed in both post-treatment tests.

次要结局

  • Exercise Endurance Time(4 weeks)
  • Inspiratory Capacity at Rest(4 weeks)
  • Ventilation at Isotime Exercise(4 weeks)
  • Intensity of "Unpleasantness of Breathing" at Isotime Exercise(4 weeks)
  • Inspiratory Capacity at Isotime Exercise(4 weeks)
  • Diaphragm Electromyogram (EMGdi) at Isotime Exercise(4 weeks)
  • Tidal Esophageal Pressure (Pes) Swings at Isotime Exercise(4 weeks)
  • Mean Expiratory Flow at Isotime Exercise(4 weeks)
  • Forced Expiratory Volume in 1 Second (FEV1)(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Denis O'Donnell

Principal Investigator

Queen's University

研究点 (1)

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