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Automatic Oxygen Titration in Patients After SARS-CoV-2 Infection

Primary Purpose

Post-COVID19

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Oxygen therapy
Sponsored by
Schön Klinik Berchtesgadener Land
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-COVID19 focused on measuring post SARS-CoV-2 infection, long-term oxygen therapy, automatic oxygen-titration, hypoxemia

Eligibility Criteria

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

Inclusion Criteria:

  • validated COVID19 disease in case history
  • hypoxemia (PO2 < 55 mmHg) under room air conditions (rest or during exercise) or SpO2 <88% during exercise
  • already established Long-term oxygen therapy or given indication for a Long-term oxygen therapy

Exclusion Criteria:

  • acute infection
  • cardiovascular diseases that limit physical fitness
  • orthopedic diseases preventing the patient from undergoing the walking tests

Sites / Locations

  • Klinikum Berchtesgadener Land, Schön Kliniken

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

ESWT Order A and B

ESWT Order B and A

Stairs Order A and B

Stairs Order B and A

Arm Description

First Endurance Shuttle Walk Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2, the second Endurance Shuttle Walk Test using the prescribed constant flow oxygen therapy.

First Endurance Shuttle Walk Test using the prescribed constant flow oxygen therapy, the second Endurance Shuttle Walk Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2.

First Stair Walking Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2, the second Stair Walking Test using the prescribed constant flow oxygen therapy.

First Stair Walking Test using the prescribed constant flow oxygen therapy, the second Stair Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2.

Outcomes

Primary Outcome Measures

Change of oxygen saturation during the endurance shuttle walk Tests
SpO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)

Secondary Outcome Measures

Change of transcutaneous pCO2 during ESWTs
tc pCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of heart rate during ESWTs and stair walking tests
Heart rate measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of respiratory rate during ESWTs
Respiratory rate measured by ApneaLink Air™
Change of time to desaturation (SpO2 ≤ 90%) and to severe desaturation (SpO2 ≤ 85%) during ESWTs and Stair Walking Tests
SpO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland) and O2matic Device.
Change of Endurance time (s)
Change of Walking Duration during the ESWT and Stair Walking Tests
Change of capillary partial pressure of CO2 (pCO2) during endurance shuttle walk tests
pCO2 measured by capillary blood gases taken before and after the ESWT
Change of capillary partial pressure of O2 (pO2) during endurance shuttle walk tests
pO2 measured by capillary blood gases taken before and after the ESWT
Patients preference due to oxygen delivery system
Patients will be asked to rate their experienced comfort after each ESWT
Change of number of stairs
Change of the number of stairs the patient was able to climb during Stair Walking Tests

Full Information

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

Unique Protocol Identification Number
NCT04849598
Brief Title
Automatic Oxygen Titration in Patients After SARS-CoV-2 Infection
Official Title
Effects of an Automatic Oxygen Titration vs. Constant Oxygen Flow Rates During Daily Activities in Patients After SARS-CoV-2 Infection
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
April 13, 2021 (Actual)
Primary Completion Date
August 27, 2021 (Actual)
Study Completion Date
August 27, 2021 (Actual)

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

5. Study Description

Brief Summary
With the progression of the SARS-CoV-2 pandemic there's an increasing number of patients recovering from COVID19. Some of these patients still experience hypoxemia and therefore are still in need of a long-term oxygen therapy (LTOT), usually provided as a constant-flow. However, during a patient's daily activities, oxygenation levels may vary and the same constant flow may not be suitable for all tasks. Studies in COPD patients suggest that an automatic oxygen titration, which adjusts the oxygen flow automatically according to a patient's blood oxygen levels to prevent desaturations, could be beneficial compared to a constant oxygen titration during exercise. So far there are no studies available that directly compare the automatic oxygen titration with the patient's prescribed constant oxygen flow in patients with hypoxemia after SARS-CoV-2 infection during activities of daily life. Therefore, the primary outcome of this study is to investigate the effects of an automatic oxygen titration (O2matic, Denmark) in comparison to constant oxygen flow rates as prescribed according to guidelines.
Detailed Description
Rationale After an infection with SARS-CoV-2, some patients still experience hypoxemia even after being discharged from the hospital. Long-term oxygen therapy (LTOT) is then used to increase the patients blood oxygen level and prolong the time spent within the SpO2 target range, decreasing the probability of severe hypoxemia or at least lowering the time spent in this severe hypoxemia and all in all enhance the patient's endurance. A prescription for LTOT is usually given for constant flow rates which might vary during day- and night use. This study is a randomized, controlled cross-over trial. Its aim is to investigate the effects of an automatic oxygen titration in patients after SARS-CoV-2 infection on the blood oxygen saturation level during activities of daily life (walking). Secondary, the effects of using an automatic titration on endurance, pCO2 blood level as well as heart rate and breathing frequency are compared to using the prescribed constant flow oxygen therapy. Design: Each patient undergoes a series of shuttle walk tests. After an initial incremental shuttle walk test (ISWT) to determine the patient's maximum walking speed, the patient undergoes 2 endurance shuttle walk tests (ESWTs) at 85% of the maximum walking speed. One of these ESWTs is performed with the prescribed constant oxygen flow, the other with the O2matic automatic oxygen titration in a random order. In addition to the shuttle walk tests, patient will perform two stair walking tests, again one with the prescribed constant oxygen flow, the other with the O2matic automatic oxygen titration in a random order. Furthermore, patients will be asked to rate their experienced comfort after each ESWT and to name their preferred oxygen titration system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-COVID19
Keywords
post SARS-CoV-2 infection, long-term oxygen therapy, automatic oxygen-titration, hypoxemia

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
ESWT Order A and B
Arm Type
Experimental
Arm Description
First Endurance Shuttle Walk Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2, the second Endurance Shuttle Walk Test using the prescribed constant flow oxygen therapy.
Arm Title
ESWT Order B and A
Arm Type
Experimental
Arm Description
First Endurance Shuttle Walk Test using the prescribed constant flow oxygen therapy, the second Endurance Shuttle Walk Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2.
Arm Title
Stairs Order A and B
Arm Type
Experimental
Arm Description
First Stair Walking Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2, the second Stair Walking Test using the prescribed constant flow oxygen therapy.
Arm Title
Stairs Order B and A
Arm Type
Experimental
Arm Description
First Stair Walking Test using the prescribed constant flow oxygen therapy, the second Stair Test using the automatic oxygen titration (O2matic) with the target range being 90 - 94% SpO2.
Intervention Type
Other
Intervention Name(s)
Oxygen therapy
Intervention Description
Oxygen therapy during ESWTs and Stair Walking Test: one test using the prescribed constant oxygen flow and one using an automatic oxygen titration system. SpO2 target range: 90 - 94%
Primary Outcome Measure Information:
Title
Change of oxygen saturation during the endurance shuttle walk Tests
Description
SpO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Day 2, 3
Secondary Outcome Measure Information:
Title
Change of transcutaneous pCO2 during ESWTs
Description
tc pCO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Day 2, 3
Title
Change of heart rate during ESWTs and stair walking tests
Description
Heart rate measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
Day 2, 3, 4
Title
Change of respiratory rate during ESWTs
Description
Respiratory rate measured by ApneaLink Air™
Time Frame
Day 2, 3
Title
Change of time to desaturation (SpO2 ≤ 90%) and to severe desaturation (SpO2 ≤ 85%) during ESWTs and Stair Walking Tests
Description
SpO2 measured by continuous transcutaneous recording via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland) and O2matic Device.
Time Frame
Day 2, 3, 4
Title
Change of Endurance time (s)
Description
Change of Walking Duration during the ESWT and Stair Walking Tests
Time Frame
Day 2, 3, 4
Title
Change of capillary partial pressure of CO2 (pCO2) during endurance shuttle walk tests
Description
pCO2 measured by capillary blood gases taken before and after the ESWT
Time Frame
Day 2, 3
Title
Change of capillary partial pressure of O2 (pO2) during endurance shuttle walk tests
Description
pO2 measured by capillary blood gases taken before and after the ESWT
Time Frame
Day 2,3
Title
Patients preference due to oxygen delivery system
Description
Patients will be asked to rate their experienced comfort after each ESWT
Time Frame
Day 3
Title
Change of number of stairs
Description
Change of the number of stairs the patient was able to climb during Stair Walking Tests
Time Frame
Day 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: validated COVID19 disease in case history hypoxemia (PO2 < 55 mmHg) under room air conditions (rest or during exercise) or SpO2 <88% during exercise already established Long-term oxygen therapy or given indication for a Long-term oxygen therapy Exclusion Criteria: acute infection cardiovascular diseases that limit physical fitness orthopedic diseases preventing the patient from undergoing the walking tests
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas R Koczulla, Prof. Dr. med.
Organizational Affiliation
Philipps University Marburg Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Klinikum Berchtesgadener Land, Schön Kliniken
City
Schönau a.Königssee
State/Province
Bavaria
ZIP/Postal Code
83471
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
27794080
Citation
Lellouche F, L'Her E, Bouchard PA, Brouillard C, Maltais F. Automatic Oxygen Titration During Walking in Subjects With COPD: A Randomized Crossover Controlled Study. Respir Care. 2016 Nov;61(11):1456-1464. doi: 10.4187/respcare.04406. Epub 2016 Oct 18.
Results Reference
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PubMed Identifier
25359356
Citation
Singh SJ, Puhan MA, Andrianopoulos V, Hernandes NA, Mitchell KE, Hill CJ, Lee AL, Camillo CA, Troosters T, Spruit MA, Carlin BW, Wanger J, Pepin V, Saey D, Pitta F, Kaminsky DA, McCormack MC, MacIntyre N, Culver BH, Sciurba FC, Revill SM, Delafosse V, Holland AE. An official systematic review of the European Respiratory Society/American Thoracic Society: measurement properties of field walking tests in chronic respiratory disease. Eur Respir J. 2014 Dec;44(6):1447-78. doi: 10.1183/09031936.00150414. Epub 2014 Oct 30.
Results Reference
background
PubMed Identifier
32217783
Citation
Prieur G, Combret Y, Medrinal C, Arnol N, Bonnevie T, Gravier FE, Quieffin J, Lamia B, Reychler G, Borel JC. Energy conservation technique improves dyspnoea when patients with severe COPD climb stairs: a randomised crossover study. Thorax. 2020 Jun;75(6):510-512. doi: 10.1136/thoraxjnl-2019-214295. Epub 2020 Mar 26.
Results Reference
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Automatic Oxygen Titration in Patients After SARS-CoV-2 Infection

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