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Carbon Dioxide Rebreathing During Exercise Assisted by Non-invasive Ventilation

Evaluation of Carbon Dioxide Rebreathing During Exercise Assisted by Non-invasive Ventilation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02655484
Enrollment
18
Registered
2016-01-14
Start date
2016-01-31
Completion date
2016-05-31
Last updated
2016-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Keywords

COPD, noninvasive ventilation, exercise, CO2 rebreathing

Brief summary

The purpose of this study was to evaluate whether CO2 rebreathing occurs in healthy subjects or patients with COPD ventilated during exercise assisted by the single-limb circuit with a plateau exhalation valve at a given inspiratory positive airway pressure and a minimal level of expiratory positive airway pressure (EPAP) and whether there is a potential threshold for predicting CO2 rebreathing.

Detailed description

Non-invasive ventilation circuit consists of single-limb tubing for inspiration and expiration, including a plateau exhalation valve. As exhaled gases was vented out the plateau exhalation valve at a constant rate, during exercise, with the increase of exhalation flow, single-limb circuit with a plateau exhalation valve might cause carbon dioxide(CO2) rebreathing. Therefore, our aim in the present study was to evaluate whether CO2 rebreathing occurs in COPD patients ventilated during exercise assisted by the single-limb circuit with a plateau exhalation valve and estimate a potential threshold for predicting CO2 rebreathing.

Interventions

DEVICEBiPAP® Vision® ventilator(Ventilator, Philips Respironics™ BiPAP® Vision® )

See details from arm descriptions.

Sponsors

Guangzhou Institute of Respiratory Disease
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* presented clinically stable (no exacerbation in the 4 weeks prior to study participation or with no change in medications); * physician diagnosed COPD, forced expiratory volume in 1s (FEV1) \< 50% predicted; * dyspnea as a main symptom that limited daily activities.

Exclusion criteria

* subjects with obvious pulmonary bullae demonstrated by chest CT scan or X-ray; * examination or facial trauma/malformation, recent facial, upper airway or upper gastrointestinal tract surgery, that would preclude receiving NIV therapy; * a history of coronary artery disease or cardiac arrhythmias or potential electrocardiographic alterations; * a history of uncontrolled hypertension, or other respiratory diseases; * oxygen saturation(SpO2) \< 88% at rest with a fraction of inspired oxygen (FiO2) ≥ 0.5; * patients with musculoskeletal or neurological disorders; * or failure to comply with the research protocol.

Design outcomes

Primary

MeasureTime frame
mean exhalation valve flowMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.

Secondary

MeasureTime frame
mean inspiratory fraction of CO2 for each tidal volumeMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
fraction of end-tidal carbon dioxide partial pressureMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
inspiratory timeMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
mean exhalation flowMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
respiratory rateMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
inspiratory tidal volumeMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
expiratory tidal volumeMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.
expiratory timeMeasurements were collected continuously throughout a symptom-limited cycle exercise test (test lasts for about 8-12 min) while subjects breathed through the full face mask. Analyses were made breath by breath during the whole test process.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026