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Completed

NCT Number: NCT00974220

Effect of Inhaled Fentanyl on Dyspnea and Exercise Tolerance in Chronic Obstructive Pulmonary Disease (COPD)

Breathing discomfort (dyspnea) and activity limitation are dominant symptoms of chronic obstructive pulmonary disease (COPD) and contribute to poor health-related quality of life in this population. Several small, uncontrolled studies and published case reports have provided evidence that inhaled fentanyl, a powerful pain relieving (opioid) medication, may be used to effectively reduce breathing discomfort in patients with advanced disease. However, the mechanisms of this improvement remain unclear. Therefore, the investigators plan to conduct the first randomized, double-blind, placebo-controlled, crossover study designed to explore the possible mechanisms of action of inhaled fentanyl on activity-related dyspnea and exercise performance in patients with advanced COPD.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Respiratory Investigation Unit, Kingston General Hospital

Kingston, Ontario, K7L 2V7, Canada

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, FEV1/forced vital capacity (FVC) ratio <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;
  • A cigarette smoking history ≥20 pack-years;
  • Significant chronic activity-related dyspnea as defined by a Baseline Dyspnea Index focal score ≤ 6;
  • Body mass index (BMI) between 18.5 and 30.0 kg/m2;
  • Able to perform all study procedures and provide/sign informed consent.

Exclusion criteria

  • A diffusing capacity of the lung for carbon monoxide (DLCO) <40 %predicted;
  • Presence of active cardiopulmonary disease other than COPD that could contribute to dyspnea and exercise limitation;
  • Clinical diagnosis of sleep disordered breathing;
  • A history/clinical evidence of asthma, atopy and/or nasal polyps;
  • History of allergy or adverse reaction to fentanyl;
  • Presence of important contraindications to clinical exercise testing, including inability to exercise because of neuromuscular or musculoskeletal disease(s);
  • Use of daytime oxygen or exercise-induced arterial oxygen desaturation to <80% on room air;
  • Use of antidepressant drugs (i.e., monoamine oxidase inhibitors, serotonin reuptake inhibitors) in previous 2 weeks;
  • Use of opioid or pain relieving drugs (e.g., morphine, fentanyl, oxycodone, hydromorphone, methadone, levorphanol, codeine, hydrocodone, meperidine) in previous 4 weeks.

Treatment and study plan

Fentanyl

Drug

single dose, 50 mcg of nebulized fentanyl citrate

Normal saline (placebo)

Drug

single dose, 0.9% saline solution

Primary outcomes

  1. Dyspnea Intensity Measured by the 10-point Borg Scale During Cycle Exercise

    Time frame: 10-minutes post-treatment

    The 10-point Borg scale ranges from 0 "nothing at all" to 10 "maximal/extremely strong" and was used to rate the intensity of dyspnea during exercise; therefore, a decrease in this rating signifies an improvement. Dyspnea intensity was assessed at the highest equivalent standardized time achieved in both post-treatment constant work rate cycle exercise tests.

Secondary outcomes

  1. Cycle Exercise Endurance Time

    Time frame: 10-minutes post-treatment

    Constant workrate cycle endurance during tests at 75% of the peak incremental workrate

Sponsors and collaborators

Lead sponsor

Queen's University

Other

Registry information

Official study title

Effect of Inhaled Nebulized Fentanyl on Exertional Dyspnea and Exercise Tolerance in Patients With Moderate-to-severe COPD

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Sep 10, 2009
Registry last updated
Jul 12, 2019

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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