Phase 3
N=17
Effect of a New Combination Bronchodilator on Exercise in GOLD Stage II Moderate COPD
COPD
Bottom Line
View on ClinicalTrials.gov: NCT01491802 ↗Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Aug 2017
Primary outcome: Primary: Exertional Dyspnea Intensity at Isotime Exercise. — 3.9; 3.4 units on a scale — p=0.090
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- LAMA/LABA (Drug); LAMA (Drug)
- Age
- Adult, Older Adult · 40+ yrs
- Sex
- All
- Sponsor
- Queen's University
- Primary completion
- Sep 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Exertional Dyspnea Intensity at Isotime Exercise. |
3.9; 3.4 | 0.090 |
| SECONDARY Exercise Endurance Time |
7.82; 7.49 | 0.680 |
| SECONDARY Inspiratory Capacity at Rest |
2.27; 2.36 | 0.197 |
| SECONDARY Ventilation at Isotime Exercise |
44.9; 47.5 | 0.006 sig |
| SECONDARY Intensity of "Unpleasantness of Breathing" at Isotime Exercise |
4.0; 3.3 | 0.044 sig |
| SECONDARY Inspiratory Capacity at Isotime Exercise |
1.99; 2.02 | 0.573 |
| SECONDARY Diaphragm Electromyogram (EMGdi) at Isotime Exercise |
53.4; 53.5 | 0.960 |
| SECONDARY Tidal Esophageal Pressure (Pes) Swings at Isotime Exercise |
28; 28 | 0.944 |
| SECONDARY Mean Expiratory Flow at Isotime Exercise |
2.19; 2.34 | 0.028 sig |
| SECONDARY Forced Expiratory Volume in 1 Second (FEV1) |
1.56; 1.72 | — |
Summary
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.
Eligibility Criteria
Inclusion Criteria
- Stable moderate COPD
- Post-bronchodilator FEV1/FVC 2
- Cigarette smoking history at least 20 pack-years
Exclusion Criteria
- 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
Data sourced from ClinicalTrials.gov (NCT01491802). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.