Clinical trial

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

Name
DMED-1926-16
Description
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.
Trial arms
Trial start
2017-09-20
Estimated PCD
2022-03-21
Trial end
2023-03-31
Status
Completed
Phase
Early phase I
Treatment
Fentanyl Citrate
100 mcg fentanyl citrate will be inhaled via nebulizer
Arms:
Fentanyl Citrate
Other names:
Inhaled fentanyl
Combivent
0.5 mg ipratropium bromide + 2.5 mg salbutamol will be inhaled via nebulizer
Arms:
Combivent Bronchodilator
Other names:
Bronchodilator
Size
20
Primary endpoint
Dyspnea intensity measured by the 10-point Borg Scale at a standardized time during cycle exercise test
10-minutes post-treatment
Eligibility criteria
Inclusion Criteria: 1. Post-bronchodilator forced expiratory volume in 1 sec (FEV1) 30-79% predicted and FEV1/forced vital capacity (FVC) \<70% 2. 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 3. Male or female ≥40 yrs of age 4. Cigarette smoking history ≥20 pack-years 5. 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) 6. Ability to perform all study procedures and provide/sign informed consent. Exclusion Criteria: 1. Women of childbearing age who are pregnant or trying to become pregnant 2. Diffusing capacity of the lung for carbon monoxide (DLCO) value of \<40 %predicted 3. Active cardiopulmonary disease other than COPD that could contribute to dyspnea and exercise limitation 4. History/clinical evidence of asthma, atopy and/or nasal polyps 5. History of hypercapnic respiratory failure or a clinical diagnosis of sleep disordered breathing 6. History of allergy or adverse response to fentanyl 7. Important contraindications to clinical exercise testing, including inability to exercise because of neuromuscular or musculoskeletal disease(s) 8. Use of daytime oxygen or exercise-induced O2 desaturation to \< 80% on room air 9. Body mass index (BMI) \<18.5 or ≥35.0 kg/m2 10. Use of antidepressant drugs (i.e., monoamine oxidase inhibitors, serotonin reuptake inhibitors) in previous 2 weeks 11. Use of opioid drugs (e.g., morphine, fentanyl, oxycodone, codeine, etc.) in the previous 4 weeks.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'CROSSOVER', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 20, 'type': 'ACTUAL'}}
Updated at
2024-04-03

1 organization

2 products

1 indication

Product
Combivent