MedPath

Measurement of changes in ventilation at various levels of inspired carbon dioxide with two methodes.

Completed
Conditions
healthy subjects
Registration Number
NL-OMON28684
Lead Sponsor
Eijsvogel, M.M.M.; Enschede; The Netherlands
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

healthy, adult aged between 18 and 65

Exclusion Criteria

history of cardio-pulmonary disease, neuro(muscular) disease, and/or kyphoscoliosis; unable to understand and read the English or Dutch language; drug abuse; use of respiratory stimulants or depressant; and pregnant women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The main study endpoint is the reproducibility of the measurements. Sensitivity slope (L/min per kPa) of the curve is calculated by means of linear regression. To assess the repeatability of both methods, the ICC is calculated between the paired CO2 sensitivity slopes of the first and second rebreathing measurement and between the first and second steady-state measurement
Secondary Outcome Measures
NameTimeMethod
Secondary endpoints are: -The experiences of the subjects with both measurements - Duration of the measurements - Costs of the method (sum of the costs of the various part of each method + costs of one long function analyst performing the measurement) - minimal CO2 in rebreathing technique
© Copyright 2025. All Rights Reserved by MedPath