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Portable Oxygen Concentrator Signal Capture Study

Portable Oxygen Concentrator Signal Capture Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03182036
Enrollment
20
Registered
2017-06-09
Start date
2017-05-26
Completion date
2017-08-03
Last updated
2021-04-19

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

Conditions

Hypoxia

Brief summary

The main purpose of this study is to learn how patients breathe on portable oxygen concentrators (POCs), and to get feedback from patients using POCs.

Detailed description

This study aims to examine patient oxygenation levels and markers of exertion (e.g. breath rate, heart rate and breath pattern) while using a portable oxygen concentrator, with the aim to understand exercise desaturation in hypoxemic subjects.

Interventions

DEVICEPortable pulsed oxygen

Hypoxemic patients will use portable pulsed oxygen at rest, and while performing a six-minute walk test.

Sponsors

St George Hospital, Australia
CollaboratorOTHER
ResMed
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient is willing to give written informed consent * Patient can read and comprehend English * Patient is ≥ 18 years of age * Patient has moderate to severe hypoxaemia (SpO2 ≤ 92%) at rest * Patient reports shortness of breath on exertion

Exclusion criteria

* Patient has musculoskeletal impairment, or other impairment that may be the limiting factor in 6MWT * Patient has a history of a psychological illness or condition such as to interfere with the patient's ability to understand the requirements of the study * Patient has acute coronary syndrome, acute myo- or pericarditis, acute lung embolism, pulmonary infarction, acute uncontrolled heart insufficiency * Patient shows signs of acute exacerbation of underlying lung condition * Patient is deemed to be unsuitable for inclusion in the opinion of the researcher, including for the following reasons: * they do not comprehend English * they are unable to provide written informed consent * they are physically unable to comply with the protocol

Design outcomes

Primary

MeasureTime frameDescription
Oxygenation20 minutesSpO2 during rest and exercise using portable pulsed oxygen therapy

Secondary

MeasureTime frameDescription
Heart rate20 minutesHeart rate during rest and exercise using portable pulsed oxygen therapy
Nasal cannula pressure20 minutesNasal cannula pressure during rest and exercise using portable pulsed oxygen therapy

Countries

Australia

Outcome results

None listed

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