Morphine, Dyspnea, Exercise and COPD
Primary Purpose
Chronic Obstructive Pulmonary Disease
Status
Unknown status
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Morphine
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring dyspnea, COPD, exercise tolerance, opioids, morphine, single dose oral Morphine
Eligibility Criteria
Inclusion Criteria:
- sever or very sever COPD, i.e. post B2 agonist FEV1<50% predicted
- age >= 40 years
- cigarette smoking history > 2 pack yrs
- ever chronic activity-related dyspnea defined by the combination of A BDI focal score <=6, Modified MRC dyspnea scale >=3 and an OCD rating <=50
- no change in medication dosage & frequency in the preceding 6 weeks
- no hospitalization or exacerbation in the preceding 6 weeks
Exclusion Criteria:
- active cardiopulmonary disease other than COPD
- contraindication to Cardiopulmonary exercise testing
- use of daytime oxygen
- exercise-induced oxyhemoglobin desaturation to <80% on room air
- Body mass index <18.5 or >30 kg/m2
- use of antidepressant drugs in the preceding 2 weeks
- use of opioid drugs in the preceding 4 weeks
- partial pressure of carbon dioxide PCo2 of >50 mmHg on capillary blood gas
Sites / Locations
- Montreal Chest InstituteRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Morphine
Placebo
Arm Description
Patient with advance COPD who will randomly receive single dose oral Morphine
patient with advanced COPD who will receive Placebo
Outcomes
Primary Outcome Measures
improvement of dyspnea
improvement of exercise tolerance
Secondary Outcome Measures
Full Information
NCT ID
NCT01718496
First Posted
October 15, 2012
Last Updated
September 22, 2015
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
1. Study Identification
Unique Protocol Identification Number
NCT01718496
Brief Title
Morphine, Dyspnea, Exercise and COPD
Official Title
Physiological Mechanisms of Dyspnea Relief and Improved Exercise Tolerance After Treatment With Oral Morphine in Patients With Advanced Chronic Obstructive Pulmonary Disease (COPD).
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Unknown status
Study Start Date
July 2014 (undefined)
Primary Completion Date
August 2016 (Anticipated)
Study Completion Date
August 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators are studying the effect of a single dose Opioid drug (Morphine) on dyspnea and exercise tolerance in COPD patients.
Detailed Description
"Dyspnea" refers to the subjective awareness of breathing discomfort that typically accompanies an increase in physical activity, particularly in patients with Chronic Obstructive Pulmonary Disease (COPD). In these patients, the symptom of dyspnea contributes significantly to exercise intolerance and an impoverished health-related quality of life. Alleviating dyspnea and improving functional capacity are, therefore, among the principal goals of COPD management, i.e., response to therapy. Nevertheless, the effective management of dyspnea and exercise intolerance remains an elusive goal for healthcare providers and current strategies aimed at reversing the patients' underlying chronic disease (e.g., bronchodilators, corticosteroids, supplemental oxygen) are only partially successful in this regard. Evidence-based clinical practice guidelines recommend that, under these circumstances, pain-relieving (opioid) medications may be used for the pharmacologic management of refractory dyspnea and activity-limitation in COPD. Indeed, a handful of published studies provide evidence to suggest that single-dose treatment with morphine or dihydrocodeine improves dyspnea and exercise performance by ~20% in patients with COPD. Nevertheless, little information is available on the physiological mechanisms by which opioid drugs contribute to these improvements in such patients. From a clinical management perspective, this information becomes crucial if we are to optimize the management of exertional symptoms in patients with advanced COPD who remain incapacitated by dyspnea, despite receiving optimal care from their healthcare provider for their underlying disease. Therefore, the purpose of the proposed randomized, double-blind, placebo-controlled, cross-over study is (1) to test the hypothesis that single-dose administration of oral morphine sulphate will improve exertional dyspnea and exercise tolerance in patients with advanced COPD and (2) elucidate the physiological underpinnings of these improvements. To this end, we will compare the effects of single-dose administration of oral morphine sulphate (0.1 mg/kg, equivalent to 7.5 mg for an average 75 kg man) and placebo on dyspnea (sensory intensity and affective responses) and exercise endurance time during symptom-limited constant-work-rate cardiopulmonary cycle exercise testing in symptomatic patients with severe-to-very severe COPD. To explore possible physiological mechanisms of symptom relief, we will measure spirometry parameters, plethysmographic lung volumes and plasma morphine concentrations; perform detailed assessments of central neural respiratory motor drive (i.e., diaphragm electromyography), contractile respiratory muscle function (i.e., esophageal, gastric and transdiaphragmatic pressures), operating lung volumes, ventilation, breathing pattern, pulmonary gas exchange and cardio-metabolic function during exercise; and employ a novel multi-dimensional evaluation technique that permits simultaneous measurement of the sensory intensity and affective dimensions of dyspnea.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
dyspnea, COPD, exercise tolerance, opioids, morphine, single dose oral Morphine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Morphine
Arm Type
Active Comparator
Arm Description
Patient with advance COPD who will randomly receive single dose oral Morphine
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
patient with advanced COPD who will receive Placebo
Intervention Type
Drug
Intervention Name(s)
Morphine
Other Intervention Name(s)
Opioids
Intervention Description
patient with advanced COPD will randomly receive single dose Morphine to assess its effect on dyspnea and exercise tolerance
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
0.9% Sodium chloride
Intervention Description
patients with advanced COPD on the other study arm will randomly receive Placebo
Primary Outcome Measure Information:
Title
improvement of dyspnea
Time Frame
one hour
Title
improvement of exercise tolerance
Time Frame
one hour
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
sever or very sever COPD, i.e. post B2 agonist FEV1<50% predicted
age >= 40 years
cigarette smoking history > 2 pack yrs
ever chronic activity-related dyspnea defined by the combination of A BDI focal score <=6, Modified MRC dyspnea scale >=3 and an OCD rating <=50
no change in medication dosage & frequency in the preceding 6 weeks
no hospitalization or exacerbation in the preceding 6 weeks
Exclusion Criteria:
active cardiopulmonary disease other than COPD
contraindication to Cardiopulmonary exercise testing
use of daytime oxygen
exercise-induced oxyhemoglobin desaturation to <80% on room air
Body mass index <18.5 or >30 kg/m2
use of antidepressant drugs in the preceding 2 weeks
use of opioid drugs in the preceding 4 weeks
partial pressure of carbon dioxide PCo2 of >50 mmHg on capillary blood gas
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dennis Jensen, Ph. D.
Phone
(514) 398-4184
Ext
0572
Email
dennis.jensen@mcgill.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Majed Alghamdi, M.D.
Phone
5149341934
Ext
32185
Email
majed.rabia@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dennis Jensen, Ph. D.
Organizational Affiliation
McGill University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montreal Chest Institute
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H2X 2P4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dennis Jensen, Ph. D.
Phone
(514) 398-4184
Ext
0572
First Name & Middle Initial & Last Name & Degree
Majed Alghamdi, M.D.
Phone
5149341934
Ext
32185
12. IPD Sharing Statement
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Morphine, Dyspnea, Exercise and COPD
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