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CO2-Patterns During Hyperoxia and Physical Exercise in COPD

Not Applicable
Conditions
COPD
Interventions
Other: Oxygen therapy
Other: Medical Air
Other: 10L/min O2
Registration Number
NCT04955561
Lead Sponsor
Schön Klinik Berchtesgadener Land
Brief Summary

The aim of the study is to investigate a possible correlation between the change in PCO2 during a hyperoxia-test and the change in PCO2 during walking in people with COPD

Detailed Description

Rationale:

Carbon dioxide partial pressure (PCO2) varies significantly in patients with advanced chronic obstructive pulmonary disease (COPD). Data from the Swedish LTOT Registry showed that PCO2 is an independent predictor for mortality and that there is a U-shaped relationship. Patients with advanced COPD who are still normocapnic at rest may still develop a clinically relevant, exercise-induced carbon dioxide (CO2) retention during exercise/ activity. It is also known that altered breathing patterns at night in COPD patients can lead to nocturnal hypercapnia, especially during REM sleep. The course of PCO2 cannot be reliably predicted by lung function parameters or resting blood gas analysis. Since exercise tests with blood gas control or nightly PCO2 monitoring are rarely performed in clinical routine, exercise induced CO2 retention often remains undetected. In the literature, there is little information on PCO2 behaviour under everyday conditions (with or without LTOT) such as rest, physical exertion and nightly sleep. Therefore, predictors that could describe the PCO2 patterns are missing. However, one former study by O'Donnel from 2002 showed that the change in CO2 under hyperoxia conditions could provide predictive information for the change in CO2 with exercise.

Objective:

Primary aim of this study is to investigate whether the change of PCO2 during a hyperoxia-test (10l/min O2 at rest) correlates with the change of PCO2 during walking exercise with either a: l/min O2 as prescribed; b: medical air; c: 10l/min O2.

Design:

This study is a randomized, controlled cross-over trial. Following an initial maximal incremental shuttle walk test (ISWT), the participant will perform 3 endurance shuttle walk tests (ESWT) at 85% of the maximum ISWT pace on three consecutive days (24h break between ESWTs). In a randomized order, participants will perform one ESWTs with O2-flow as prescribed (e.g. study day 1), one with medical air (same flow rate as prescribed oxygen) (e.g. study day 2) and one with 10l/min O2 (e.g. study day 3). An additional hyperoxia test (10l/min O2 for ten minutes; at resting condition) will be perfomed on each day prior to performing an ESWT.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
55
Inclusion Criteria
  • COPD III/ IV
  • 35mmHg < PCO2 <= 55mmHg (under resting conditions, breathing room air)
  • Hypoxemia (PaO2<60mmHg) under room air conditions (rest or during exercise) or SpO2 <88% during exercise
  • established oxygen therapy or given indication for oxygen therapy
  • written informed consent
Exclusion Criteria
  • acute exacerbation of COPD
  • exercise limiting cardiac or orthopedic comorbidites
  • PaO2 <50mmHg at rest, breathing room air

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Randomised to begin with oxygen-supplementation at 10L/min during ESWTMedical AirRandomised order of tests starting with the 10L/min O2, during the ESWT followed by prescribed O2 flow rate or medical air in randomised order on seperate days
Randomised to begin with oxygen supplementation at prescibed O2 flow rate during ESWTMedical AirRandomised order of tests starting with the prescribed O2 flow rate, during the ESWT followed by 10L/min O2 or medical air in randomised order on seperate days
Randomised to begin with oxygen-supplementation at 10L/min during ESWTOxygen therapyRandomised order of tests starting with the 10L/min O2, during the ESWT followed by prescribed O2 flow rate or medical air in randomised order on seperate days
Randomised to begin with medical air supplementation at prescibed O2 flow rate during ESWTMedical AirRandomised order of tests starting with the medical air during the ESWT followed by prescribed O2 flow rate or 10L/min O2 in randomised order on seperate days
Randomised to begin with oxygen-supplementation at 10L/min during ESWT10L/min O2Randomised order of tests starting with the 10L/min O2, during the ESWT followed by prescribed O2 flow rate or medical air in randomised order on seperate days
Randomised to begin with medical air supplementation at prescibed O2 flow rate during ESWTOxygen therapyRandomised order of tests starting with the medical air during the ESWT followed by prescribed O2 flow rate or 10L/min O2 in randomised order on seperate days
Randomised to begin with medical air supplementation at prescibed O2 flow rate during ESWT10L/min O2Randomised order of tests starting with the medical air during the ESWT followed by prescribed O2 flow rate or 10L/min O2 in randomised order on seperate days
Randomised to begin with oxygen supplementation at prescibed O2 flow rate during ESWTOxygen therapyRandomised order of tests starting with the prescribed O2 flow rate, during the ESWT followed by 10L/min O2 or medical air in randomised order on seperate days
Randomised to begin with oxygen supplementation at prescibed O2 flow rate during ESWT10L/min O2Randomised order of tests starting with the prescribed O2 flow rate, during the ESWT followed by 10L/min O2 or medical air in randomised order on seperate days
Primary Outcome Measures
NameTimeMethod
Change in PCO2 during hyperoxia at restChange from baseline to after 10 minutes breathing 10L/min oxygen

pCO2 measured by capillary blood gases taken before and after the hyperoxia test

Change in PCO2 from rest to end exercise (endurance shuttle walk test)Change from baseline to the end of the ESWT, up to 20 minutes

pCO2 measured by capillary blood gases taken before and after the ESWT

Secondary Outcome Measures
NameTimeMethod
Breathing frequency during endurance shuttle walk testContinuously during ESWT, up to 20 minutes

Breathing frequency during the ESWT measured by ApneaLink Air™ (ResMed)

Heart rate during endurance shuttle walk testContinuously during ESWT, up to 20 minutes

Heart rate measured by continuous transcutaneous recordung via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)

Transcutaneous partial pressure of CO2 (TcPCO2) during hyperoxia testContinuously from baseline to 10 minutes breathing 10L/min oxygen

TcPCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)

Transcutaneous partial pressure of CO2 (TcPCO2) during endurance shuttle walk testContinuously during ESWT, up to 20 minutes

TcPCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)

Breathing frequency during hyperoxia testContinuously from baseline to 10 minutes breathing 10L/min oxygen

Breathing frequency during the hyperoxia test measured by ApneaLink Air™ (ResMed)

Change of inspiratory capacity during endurance shuttle walk testChange from baseline to the end of the ESWT, up to 20 minutes

IC measured by SpiroSense (Pari) before and after the ESWT

Heart rate during hyperoxia testContinuously from baseline to 10 minutes breathing 10L/min oxygen

Heart rate measured by continuous transcutaneous recordung via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)

Change of capillary partial pressure of O2 (pO2) during endurance shuttle walk testChange from baseline to the end of the ESWT, up to 20 minutes

pO2 measured by capillary blood gases taken before and after the ESWT

Trial Locations

Locations (1)

Klinikum Berchtesgadener Land, Schön Kliniken

🇩🇪

Schönau am Königssee, Germany

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