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Short-term Effects of Supplemental Oxygen in Patients With IPF (IPFO2)

Primary Purpose

Idiopathic Pulmonary Fibrosis (IPF)

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Medical air
Oxygen (2Liter/min)
Oxygen (4Liter/min)
Sponsored by
Schön Klinik Berchtesgadener Land
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Pulmonary Fibrosis (IPF) focused on measuring supplemental oxygen, walking capacity, exercise capacity, endurance shuttle walk test

Eligibility Criteria

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

Inclusion criteria:

  • patients with idiopathic pulmonary fibrosis and hypoxemia at rest or during exercise (PaO2 <55 mmHg or SpO2 <88%)
  • Written informed consent

Exclusion criteria:

  • Forced vital capacity < 50% pred.
  • Clinical signs of any cardial comorbidity
  • Not able to walk
  • Oxygen flow needed during exercise > 4l/min

Sites / Locations

  • Schoen Klinik Berchtesgadener Land

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

ESWT order 1

ESWT order 2

ESWT order 3

ESWT order 4

ESWT order 5

ESWT order 6

Arm Description

Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: medical air (MA) Oxygen (2 Liter/min) Oxygen (4 Liter/min)

Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: medical air (MA) Oxygen (4 Liter/min) Oxygen (2 Liter/min)

Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (2 Liter/min) Medical air (MA) Oxygen (4 Liter/min)

Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (2 Liter/min) Oxygen (4 Liter/min) Medical air (MA)

Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (4 Liter/min) Medical air (MA) Oxygen (2 Liter/min)

Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (4 Liter/min) Oxygen (2 Liter/min) Medical air (MA)

Outcomes

Primary Outcome Measures

Endurance time (in seconds) measured by endurance shuttle walk test

Secondary Outcome Measures

Change of breathing frequency during endurance shuttle walk test
measured by NOX-T3 (NoxMedical, Reykjavik, Iceland)
Change of Oxygen saturation during endurance shuttle walk test
continuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of heart rate during endurance shuttle walk test
continuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of partial pressure of carbon dioxide during endurance shuttle walk test
continuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of inspiratory capacity during endurance shuttle walk test
measured by Spiropalm 6MWT (Cosmed, Italy)

Full Information

First Posted
November 25, 2016
Last Updated
December 3, 2018
Sponsor
Schön Klinik Berchtesgadener Land
Collaborators
Linde AG
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1. Study Identification

Unique Protocol Identification Number
NCT03050255
Brief Title
Short-term Effects of Supplemental Oxygen in Patients With IPF
Acronym
IPFO2
Official Title
Short-term Effects of Supplemental Oxygen During Walking in Hypoxemic Patients With Idiopathic Pulmonary Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
November 2016 (Actual)
Primary Completion Date
March 2018 (Actual)
Study Completion Date
March 2018 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Although exercise-induced desaturation is frequently observed in patients with idiopathic pulmonary fibrosis (IPF) short-term effects of supplemental oxygen during walking have not been investigated yet. Given, that walking ability is the most important activity of daily life, the aim of our study is to investigate the effects of supplemental oxygen on endurance walking capacity in hypoxemic IPF patients. In this study patients will perform 3 endurance shuttle walk tests (ESWTs) at 85% of their individual peak performance using medical air (=compressed room air, 2 liters/minute), 2 liters/minute oxygen, 4 liters/minute Oxygen in a double-blinded fashion and random order. Since there are only limited pharmacological treatment options for IPF patients, this study may help to provide novel information about the short-term effects of supplemental oxygen. Furthermore it may help to investigate possibilities to optimize oxygen therapy in order to facilitate patients´ participation in activities of daily life and not at least to improve patients´ quality of life.
Detailed Description
Rationale: Exercise-induced desaturation is frequently observed in patients with idiopathic pulmonary fibrosis and predicts poorer outcomes. However, prospective studies with larger sample sizes and those investigating the effect of oxygen on endurance time, oxygen saturation and breathing frequency during walking are lacking. Given that walking is the most important activity of daily life to preserve the maintenance and to participate in social life, we aim to investigate the effects of supplemental oxygen during walking in IPF patients. The endurance shuttle walk test (ESWT) is a well validated test with high reliability and validity for measuring endurance walking capacity in patients with chronic obstructive pulmonary disease (COPD). The advantage of this test in contrast to the 6-minute walk test is that the ESWT is performed at 85% of the individual maximum that is close to the intensity of typical daily activities. Additionally, by using the ESWT it is possible to determine the maximum duration of exercise and to compare values at isotime (= time point when the shortest of the 3 ESWTs ends), whereas values at the end of different six-minute walk tests (6MWTs) are not comparable in case of different distances. Aim: To investigate the short-term effects of supplemental oxygen on endurance capacity during walking (ESWT) in patients with idiopathic pulmonary fibrosis. Design: This study is a randomized, controlled, double-blinded cross-over trial. Following an initial incremental shuttle walk test (ISWT) in order to determine the individual maximum walking capacity, patients will perform 3 endurance shuttle walk tests (ESWT) at 85% of the maximal pace. In randomized order, patients will complete one ESWT on 2l/min oxygen, one on 4l/min oxygen and one on medical air (=compressed room air), whereas the patients as well as the investigator will be blinded to the gas mixture provided. All 3 conditions will be provided via nasal cannula. The time between the two ESWTs will be 24 hours in order to give enough time for regeneration. Endurance Walking capacity as measured by the ESWT will be used as the primary outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Fibrosis (IPF)
Keywords
supplemental oxygen, walking capacity, exercise capacity, endurance shuttle walk test

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ESWT order 1
Arm Type
Experimental
Arm Description
Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: medical air (MA) Oxygen (2 Liter/min) Oxygen (4 Liter/min)
Arm Title
ESWT order 2
Arm Type
Experimental
Arm Description
Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: medical air (MA) Oxygen (4 Liter/min) Oxygen (2 Liter/min)
Arm Title
ESWT order 3
Arm Type
Experimental
Arm Description
Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (2 Liter/min) Medical air (MA) Oxygen (4 Liter/min)
Arm Title
ESWT order 4
Arm Type
Experimental
Arm Description
Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (2 Liter/min) Oxygen (4 Liter/min) Medical air (MA)
Arm Title
ESWT order 5
Arm Type
Experimental
Arm Description
Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (4 Liter/min) Medical air (MA) Oxygen (2 Liter/min)
Arm Title
ESWT order 6
Arm Type
Experimental
Arm Description
Subject performs endurance shuttle walk tests (ESWT) under following conditions in the following order: Oxygen (4 Liter/min) Oxygen (2 Liter/min) Medical air (MA)
Intervention Type
Other
Intervention Name(s)
Medical air
Intervention Type
Other
Intervention Name(s)
Oxygen (2Liter/min)
Intervention Type
Other
Intervention Name(s)
Oxygen (4Liter/min)
Primary Outcome Measure Information:
Title
Endurance time (in seconds) measured by endurance shuttle walk test
Time Frame
Time until Patient terminates ESWT due to leg fatigue or dyspnea, up to 20 minutes
Secondary Outcome Measure Information:
Title
Change of breathing frequency during endurance shuttle walk test
Description
measured by NOX-T3 (NoxMedical, Reykjavik, Iceland)
Time Frame
change from baseline to the end of the ESWT, up to 20 minutes
Title
Change of Oxygen saturation during endurance shuttle walk test
Description
continuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
change from baseline to the end of the ESWT, up to 20 minutes
Title
Change of heart rate during endurance shuttle walk test
Description
continuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Time Frame
change from baseline to the end of the ESWT, up to 20 minutes
Title
Change of partial pressure of carbon dioxide during endurance shuttle walk test
Description
continuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
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
measured by Spiropalm 6MWT (Cosmed, Italy)
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: patients with idiopathic pulmonary fibrosis and hypoxemia at rest or during exercise (PaO2 <55 mmHg or SpO2 <88%) Written informed consent Exclusion criteria: Forced vital capacity < 50% pred. Clinical signs of any cardial comorbidity Not able to walk Oxygen flow needed during exercise > 4l/min
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Klaus Kenn, Prof.
Organizational Affiliation
Schoen Klinik Berchtesgadener Land
Official's Role
Principal Investigator
Facility Information:
Facility Name
Schoen Klinik Berchtesgadener Land
City
Schönau Am Königssee
ZIP/Postal Code
83471
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Short-term Effects of Supplemental Oxygen in Patients With IPF

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