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SpO2 Measurement Depending on Different Pulse Oximeter Averaging Time Settings

SpO2 Measurement Depending on Different Pulse Oximeter Averaging Time Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04933773
Enrollment
17
Registered
2021-06-22
Start date
2021-05-15
Completion date
2021-10-15
Last updated
2022-01-28

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

Conditions

Movement Artifacts During SpO2 Measurements, Reduced Perfusion During SpO2 Measurements

Keywords

pulse oximetry, SpO2, averaging time, motion artifacts

Brief summary

The aim of this study is to characterize the noise in the SpO2 signal depending on different pulse oximeter averaging time settings.

Detailed description

Noise in the SpO2 signal is most often caused by artifacts, such as movement artifacts, reduced perfusion, additional light and others. These artifacts can be partially removed from the SpO2 signal by different pulse oximeter settings, specifically the sensitivity mode and averaging time. It is known that when a longer averaging time is set, the measured signal contains fewer artifacts, on the other hand there is an increased risk of missing short desaturation. The aim of this work is to characterize the noise in the SpO2 signal depending on the set averaging time of the pulse oximeter based on experimental data from healthy volunteers.

Interventions

OTHERMovement artifact - knocking

60 seconds motion artifact simulation - knocking with sensors

OTHERMovement artifact - tremor

60 seconds motion artifact simulation - tremor with sensors

OTHERArtifact - ambient light

60 seconds artifact simulation - ambient light using sensor opening

OTHERArtifact - low perfusion

60 seconds artifact simulation - reduced perfusion using a cuff

Two SpO2 measuring devices are active simultaneously on one hand during measurement.

Sponsors

Czech Technical University in Prague
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Intervention model description

All participants go through all study arms, in random order. Two pulse oximeters with different averaging time settings are active simultaneously during measurement on each participant and the measured signal is compared.

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers from the Czech Technical University

Exclusion criteria

* pregnancy * severe cardiovascular conditions * injury to the upper limbs or hands that could affect the peripheral perfusion * diabetes * hypotension or hypertension

Design outcomes

Primary

MeasureTime frameDescription
SpO2 readings with different averaging times30 minutesDifferences in the SpO2 signal during artifacts depending on the set averaging time.

Countries

Czechia

Outcome results

None listed

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