Skip to content

Short-term Effects of Supplemental Oxygen in Patients With IPF

Short-term Effects of Supplemental Oxygen During Walking in Hypoxemic Patients With Idiopathic Pulmonary Fibrosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03050255
Acronym
IPFO2
Enrollment
53
Registered
2017-02-10
Start date
2016-11-30
Completion date
2018-03-31
Last updated
2018-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Pulmonary Fibrosis (IPF)

Keywords

supplemental oxygen, walking capacity, exercise capacity, endurance shuttle walk test

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.

Interventions

OTHERMedical air
OTHEROxygen (2Liter/min)
OTHEROxygen (4Liter/min)

Sponsors

Linde AG
CollaboratorINDUSTRY
Schön Klinik Berchtesgadener Land
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Endurance time (in seconds) measured by endurance shuttle walk testTime until Patient terminates ESWT due to leg fatigue or dyspnea, up to 20 minutes

Secondary

MeasureTime frameDescription
Change of breathing frequency during endurance shuttle walk testchange from baseline to the end of the ESWT, up to 20 minutesmeasured by NOX-T3 (NoxMedical, Reykjavik, Iceland)
Change of Oxygen saturation during endurance shuttle walk testchange from baseline to the end of the ESWT, up to 20 minutescontinuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of heart rate during endurance shuttle walk testchange from baseline to the end of the ESWT, up to 20 minutescontinuous 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 testChange from baseline to the end of the ESWT, up to 20 minutescontinuous transcutaneous recording during endurance shuttle walk test via Sentec-Digital Monitor® (Sentec, Therwil, Switzerland)
Change of inspiratory capacity during endurance shuttle walk testChange from baseline to the end of the ESWT, up to 20 minutesmeasured by Spiropalm 6MWT (Cosmed, Italy)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026