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CO2-Patterns During Hyperoxia and Physical Exercise in COPD

Primary Purpose

COPD

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Oxygen therapy
Medical Air
10L/min O2
Sponsored by
Schön Klinik Berchtesgadener Land
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COPD focused on measuring CO2, oxygen, walking exercise

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Klinikum Berchtesgadener Land, Schön KlinikenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Randomised to begin with oxygen-supplementation at 10L/min during ESWT

Randomised to begin with medical air supplementation at prescibed O2 flow rate during ESWT

Randomised to begin with oxygen supplementation at prescibed O2 flow rate during ESWT

Arm Description

Randomised 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 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 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

Outcomes

Primary Outcome Measures

Change in PCO2 during hyperoxia at rest
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)
pCO2 measured by capillary blood gases taken before and after the ESWT

Secondary Outcome Measures

Transcutaneous partial pressure of CO2 (TcPCO2) during hyperoxia test
TcPCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Transcutaneous partial pressure of CO2 (TcPCO2) during endurance shuttle walk test
TcPCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Breathing frequency during hyperoxia test
Breathing frequency during the hyperoxia test measured by ApneaLink Air™ (ResMed)
Breathing frequency during endurance shuttle walk test
Breathing frequency during the ESWT measured by ApneaLink Air™ (ResMed)
Heart rate during endurance shuttle walk test
Heart rate measured by continuous transcutaneous recordung via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Heart rate during hyperoxia test
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 test
pO2 measured by capillary blood gases taken before and after the ESWT
Change of inspiratory capacity during endurance shuttle walk test
IC measured by SpiroSense (Pari) before and after the ESWT

Full Information

First Posted
May 4, 2021
Last Updated
July 13, 2021
Sponsor
Schön Klinik Berchtesgadener Land
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1. Study Identification

Unique Protocol Identification Number
NCT04955561
Brief Title
CO2-Patterns During Hyperoxia and Physical Exercise in COPD
Official Title
CO2-Patterns During Hyperoxia and Physical Exercise in People With Severe COPD - a Randomized, Double-blind Cross Over Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 13, 2021 (Actual)
Primary Completion Date
May 2022 (Anticipated)
Study Completion Date
May 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Schön Klinik Berchtesgadener Land

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD
Keywords
CO2, oxygen, walking exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
55 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Randomised to begin with oxygen-supplementation at 10L/min during ESWT
Arm Type
Experimental
Arm Description
Randomised 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
Arm Title
Randomised to begin with medical air supplementation at prescibed O2 flow rate during ESWT
Arm Type
Experimental
Arm Description
Randomised 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
Arm Title
Randomised to begin with oxygen supplementation at prescibed O2 flow rate during ESWT
Arm Type
Experimental
Arm Description
Randomised 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
Intervention Type
Other
Intervention Name(s)
Oxygen therapy
Intervention Description
Supplemental O2 at rest of 10 l/min for ten minutes followed by supplemental O2 at the prescribed exercise O2-flow rate during ESWT.
Intervention Type
Other
Intervention Name(s)
Medical Air
Intervention Description
Supplemental O2 at rest of 10 l/min for ten minutes followed by medical Air at prescribed O2 flow rate during ESWT.
Intervention Type
Other
Intervention Name(s)
10L/min O2
Intervention Description
Supplemental O2 at rest of 10 l/min for ten minutes followed by 10L/min O2 during ESWT.
Primary Outcome Measure Information:
Title
Change in PCO2 during hyperoxia at rest
Description
pCO2 measured by capillary blood gases taken before and after the hyperoxia test
Time Frame
Change from baseline to after 10 minutes breathing 10L/min oxygen
Title
Change in PCO2 from rest to end exercise (endurance shuttle walk test)
Description
pCO2 measured by capillary blood gases taken before and after the ESWT
Time Frame
Change from baseline to the end of the ESWT, up to 20 minutes
Secondary Outcome Measure Information:
Title
Transcutaneous partial pressure of CO2 (TcPCO2) during hyperoxia test
Description
TcPCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Continuously from baseline to 10 minutes breathing 10L/min oxygen
Title
Transcutaneous partial pressure of CO2 (TcPCO2) during endurance shuttle walk test
Description
TcPCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Continuously during ESWT, up to 20 minutes
Title
Breathing frequency during hyperoxia test
Description
Breathing frequency during the hyperoxia test measured by ApneaLink Air™ (ResMed)
Time Frame
Continuously from baseline to 10 minutes breathing 10L/min oxygen
Title
Breathing frequency during endurance shuttle walk test
Description
Breathing frequency during the ESWT measured by ApneaLink Air™ (ResMed)
Time Frame
Continuously during ESWT, up to 20 minutes
Title
Heart rate during endurance shuttle walk test
Description
Heart rate measured by continuous transcutaneous recordung via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Continuously during ESWT, up to 20 minutes
Title
Heart rate during hyperoxia test
Description
Heart rate measured by continuous transcutaneous recordung via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Continuously from baseline to 10 minutes breathing 10L/min oxygen
Title
Change of capillary partial pressure of O2 (pO2) during endurance shuttle walk test
Description
pO2 measured by capillary blood gases taken before and after the ESWT
Time Frame
Change from baseline to the end of the ESWT, up to 20 minutes
Title
Change of inspiratory capacity during endurance shuttle walk test
Description
IC measured by SpiroSense (Pari) before and after the ESWT
Time Frame
Change from baseline to the end of the ESWT, up to 20 minutes

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tessa Schneeberger
Phone
+498652931540
Ext
+498652931540
Email
TSchneeberger@Schoen-Klinik.de
Facility Information:
Facility Name
Klinikum Berchtesgadener Land, Schön Kliniken
City
Schönau am Königssee
ZIP/Postal Code
83471
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tessa Schneeberger, MSc
Phone
0049 - 8652 - 932730
Email
tschneeberger@schoen-klinik.de

12. IPD Sharing Statement

Plan to Share IPD
Yes

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CO2-Patterns During Hyperoxia and Physical Exercise in COPD

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