Chronic Obstructive Pulmonary Disease Clinical Trial
Official title:
Effects of Automated Oxygen Titration Alone or With High Flow Nasal Therapy on Dyspnea and Exercise Tolerance in Patients With Desaturating Chronic Lung Disease: a Randomized Clinical Trial
NCT number | NCT05267418 |
Other study ID # | 21726 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | February 26, 2019 |
Est. completion date | March 30, 2021 |
Verified date | March 2022 |
Source | Laval University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of this study is to evaluate the effects of automated oxygen administration (FreeO2 system) alone or with high-flow oxygen on dyspnea and exercise tolerance in people with desaturating chronic lung disease compared to fixed oxygen therapy.
Status | Terminated |
Enrollment | 30 |
Est. completion date | March 30, 2021 |
Est. primary completion date | March 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: One of them - Moderate to severe COPD (forced expiratory volume in 1 second (FEV1) < 80% predicted and FEV1/forced vital capacity (FVC) ratio < 0.7) - Chronic interstitial lung disease such as usual interstitial pneumonitis (UIP), non-specific interstitial pneumonitis (NSIP) or hypersensitivity pneumonitis on high-resolution computed tomography - Pulmonary arterial hypertension type 1 or 4, excluding involvement secondary to collagenosis as well as secondary to congenital heart disease, as diagnosed with mean pulmonary artery pressure > 25 mm Hg at right heart catheterization - Cystic fibrosis, as diagnosed by a positive sweat test (>60 mmol/L) or having 2 genetic mutations known to cause cystic fibrosis. AND having a 6-minute walking test with significant desaturation defined as a decrease in O2 saturation greater or equal to 5% with O2 saturation at the end of the walking test < 88% Exclusion Criteria: - Exacerbation of the primary lung disease in the past 8 weeks - Exercise limiting diseases other than the primary lung disease. - Not reaching the target dyspnea score during the walking tests. - Stage 1 pulmonary sarcoidosis - History of syncope on exertion - SpO2 with effort less than 90% despite the use of 6 L of O2 per minute - Cardiac condition deemed unstable or severe (e.g. severe aortic stenosis) - Disabling or severe rheumatological or neurological condition - Participation in a pulmonary rehabilitation program within the last year - Patients with multi-resistant bacteria |
Country | Name | City | State |
---|---|---|---|
Canada | Institut Universitaire de Cardiologie et de Pneumologie de Québec | Québec | Quebec |
Lead Sponsor | Collaborator |
---|---|
Laval University |
Canada,
Beaulieu J, Jensen D, O'Donnell DE, Brouillard C, Tracey L, Vincent S, Nadreau É, Bernard E, Bernard S, Maltais F. Relieving exertional dyspnea during the 3-min constant speed shuttle test in patients with COPD with indacaterol/glycopyrronium versus tiotropium: the RED trial. Ther Adv Respir Dis. 2020 Jan-Dec;14:1753466620939507. doi: 10.1177/1753466620939507. — View Citation
Maltais F, Aumann JL, Kirsten AM, Nadreau É, Macesic H, Jin X, Hamilton A, O'Donnell DE. Dual bronchodilation with tiotropium/olodaterol further reduces activity-related breathlessness versus tiotropium alone in COPD. Eur Respir J. 2019 Mar 28;53(3). pii: 1802049. doi: 10.1183/13993003.02049-2018. Print 2019 Mar. — View Citation
Perrault H, Baril J, Henophy S, Rycroft A, Bourbeau J, Maltais F. Paced-walk and step tests to assess exertional dyspnea in COPD. COPD. 2009 Oct;6(5):330-9. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Mean pulsed O2 saturation (SpO2) during 3min-CSST | The mean % pulsed O2 saturation (SpO2) during the test duration time | From the beginning to the end of the 3 minute-constant speed shuttle test which will be done on 3 testing days with either fixed O2, automatic O2 adjustment alone, or automatic O2 adjustment + high nasal flow) | |
Other | Capillary blood gases | Carbon dioxide partial pressure (PCO2), lactate | Difference the baseline capillary PCO2 from the resting values (before Endurance Shuttle Walking Test - ESWT) to the end of exercise values (after the Endurance Shuttle Walking Test - ESWT) immediately after the intervention | |
Primary | Dyspnea score | Dyspnea score on the modified Borg scale (0 to 10, with higher score indicating worse dyspnea) | At the end of the 3 minute-constant speed shuttle test (CSST) (3 minutes), immediately after the intervention (either fixed-O2, automated nasal O2 adjustment alone, or automated nasal O2 adjustment + high nasal flow) | |
Secondary | Endurance time duration of the Endurance Shuttle Walking Test (EWST) | Total duration of Endurance Shuttle Walking Test | Duration in (mm:ss) of Endurance Shuttle Walking Test (ESWT), immediately after the intervention (either fixed-O2, automated nasal O2 adjustment alone, or automated nasal O2 adjustment + high nasal flow) | |
Secondary | Mean pulsed O2 saturation (SpO2) during Endurance Shuttle Walking Test (EWST) | Mean % pulsed O2 saturation (SpO2) during the Endurance Shuttle Walking Test (ESWT) | From the beginning to the end of the Endurance Shuttle Walking Test (ESWT) which will be done on 3 testing days, with either fixed O2, automatic O2 adjustment alone, or automatic O2 adjustment + high nasal flow |
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