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Completed

NCT Number: NCT03405090

Differential Mechanisms of Dyspnea Relief in Advanced COPD: Opiates vs. Bronchodilators

Activity-related breathlessness (dyspnea) is the dominant symptom and persists despite optimal medical care in as many as 50% of patients with advanced chronic obstructive pulmonary disease (COPD). The objective of this project is to determine the underlying mechanisms of the activity-related breathlessness in patients with advanced COPD. To study the different pathways involved in causing breathlessness, we will compare the effects of two treatments, opiates with oxygen versus bronchodilators, which relieve breathlessness in different ways.

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Key information

Age range

40 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Respiratory Investigation Unit

Kingston, Ontario, K7L 2V7, Canada

About this study

Dyspnea arises during exercise in COPD patients when there is a mismatch between the ventilatory demand (largely dictated by chemical stimuli) and the capacity to respond to that demand (dictated by mechanical/muscular factors). Our preliminary studies have indicated that treatment with opioids in COPD patients can improve activity related dyspnea by reducing central respiratory neural drive and breathing frequency without a significant change in the respiratory mechanics. By contrast, a reduction in exertional dyspnea following inhaled bronchodilators in COPD was mainly related to an improved respiratory mechanics with increased inspiratory capacity, tidal volume, and inspiratory reserve volume etcetera. By comparing the physiological mechanisms of dyspnea relief during the opiate and bronchodilator therapy, we hope to gain new insights into the mechanisms of dyspnea in COPD by selectively manipulating inspiratory neural drive (nebulized opiates) and abnormal respiratory mechanics (nebulized bronchodilators) within the same individuals. As such, the primary objective of this study is to compare the effects of inhaled opiate with oxygen versus bronchodilator treatments on the intensity of dyspnea, electromyographic estimates of inspiratory neural drive and respiratory mechanics and their interactions during a standardized exercise test using a randomized, controlled, crossover design in patients with COPD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Post-bronchodilator forced expiratory volume in 1 sec (FEV1) 30-79% predicted and FEV1/forced vital capacity (FVC) <70%
  • Clinically stable as defined by no changes in medication dosage or frequency of administration with no exacerbations or hospital admissions in the preceding 6 weeks
  • Male or female ≥40 yrs of age
  • Cigarette smoking history ≥20 pack-years
  • Moderate-to-severe chronic activity-related dyspnea as defined by a modified MRC dyspnea scale ≥2, COPD Assessment Test score ≥10 or Baseline Dyspnea Index focal score ≤6 (47-49)
  • Ability to perform all study procedures and provide/sign informed consent.

Exclusion criteria

  • Women of childbearing age who are pregnant or trying to become pregnant
  • Diffusing capacity of the lung for carbon monoxide (DLCO) value of <40 %predicted
  • Active cardiopulmonary disease other than COPD that could contribute to dyspnea and exercise limitation
  • History/clinical evidence of asthma, atopy and/or nasal polyps
  • History of hypercapnic respiratory failure or a clinical diagnosis of sleep disordered breathing
  • History of allergy or adverse response to fentanyl
  • Important contraindications to clinical exercise testing, including inability to exercise because of neuromuscular or musculoskeletal disease(s)
  • Use of daytime oxygen or exercise-induced O2 desaturation to < 80% on room air
  • Body mass index (BMI) <18.5 or ≥35.0 kg/m2
  • Use of antidepressant drugs (i.e., monoamine oxidase inhibitors, serotonin reuptake inhibitors) in previous 2 weeks
  • Use of opioid drugs (e.g., morphine, fentanyl, oxycodone, codeine, etc.) in the previous 4 weeks.

Treatment and study plan

Fentanyl Citrate

Drug

100 mcg fentanyl citrate will be inhaled via nebulizer

Other names: Inhaled fentanyl

Combivent

Drug

0.5 mg ipratropium bromide + 2.5 mg salbutamol will be inhaled via nebulizer

Other names: Bronchodilator

Primary outcomes

  1. Dyspnea intensity measured by the 10-point Borg Scale at a standardized time during cycle exercise test

    Time frame: 10-minutes post-treatment

    The 10-point Borg scale ranges from 0 "nothing at all" to 10 "maximal/extremely strong" and will be used to rate the intensity of dyspnea during exercise: a decrease in this rating signifies an improvement. Dyspnea intensity will be assessed at a standardized time (4-minutes) in both post-treatment constant-load cycle exercise tests.

Secondary outcomes

  1. Diaphragm electromyography (EMGdi) at a standardized time during cycle exercise test

    Time frame: 10-minutes post-treatment

    EMGdi will be used as an index of inspiratory neural drive. Assessments will be compared at a standardized time (4-minutes) during both post-treatment constant-load cycle exercise tests.

  2. Ventilation at a standardized time during cycle exercise test

    Time frame: 10-minutes post-treatment

    Exercise measurements of minute ventilation will be compared at a standardized time (4-minutes) during both post-treatment constant-load exercise tests.

  3. Breathing frequency at a standardized time during cycle exercise test

    Time frame: 10-minutes post-treatment

    Exercise measurements of breathing frequency (respiratory rate) will be compared at a standardized time (4-minutes) during both post-treatment constant-load exercise tests.

  4. Tidal volume at a standardized time during cycle exercise test

    Time frame: 10-minutes post-treatment

    Exercise measurements of tidal volume will be compared at a standardized time (4-minutes) during both post-treatment constant-load cycle exercise tests.

  5. Inspiratory capacity at a standardized time during cycle exercise test

    Time frame: 10-minutes post-treatment

    Exercise measurements of inspiratory capacity will be compared at a standardized time (4-minutes) during both post-treatment constant-load cycle exercise tests.

Sponsors and collaborators

Lead sponsor

Dr. Denis O'Donnell

Other

Collaborators

  • Ontario Lung Association
  • Queen's University

Registry information

Important dates

Study start
2017
Primary completion
2022
Study completion
2023
First posted
Jan 19, 2018
Registry last updated
Apr 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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