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CompletedNCT04933773Updated Jan 28, 2022

SpO2 Measurement Depending on Different Pulse Oximeter Averaging Time Settings

An interventional study of Movement artifact - knocking and Movement artifact - tremor in Movement Artifacts During SpO2 Measurements and Reduced Perfusion During SpO2 Measurements, sponsored by Czech Technical University in Prague. Completed at 1 site in Czechia. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-01-28.

Sponsored by Czech Technical University in Prague · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
17
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

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

Read the 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.

02

Conditions studied

  • Movement Artifacts During SpO2 Measurements
  • Reduced Perfusion During SpO2 Measurements

Keywords

  • pulse oximetry
  • SpO2
  • averaging time
  • motion artifacts
03

In context

Lead sponsor

Czech Technical University in Prague is the lead sponsor of 36 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • healthy volunteers from the Czech Technical University

Exclusion criteria

Exclusion Criteria:

  • pregnancy
  • severe cardiovascular conditions
  • injury to the upper limbs or hands that could affect the peripheral perfusion
  • diabetes
  • hypotension or hypertension
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
17 participants (actual)

Study arms

  • Experimental
    Set averaging times: 2-4 seconds and 8 seconds

    SpO2 is measured by two pulse oximeters on one participant's hand (on the index finger and middle finger). One pulse oximeter is set to an averaging time of 2-4 seconds, the second pulse oximeter is set to an averaging time of 8 seconds.

    Other: Movement artifact - knocking · Other: Movement artifact - tremor · Other: Artifact - ambient light · Other: Artifact - low perfusion · Other: SpO2 measurement

  • Experimental
    Set averaging times: 8 seconds and 16 seconds

    SpO2 is measured by two pulse oximeters on one participant's hand (on the index finger and middle finger). One pulse oximeter is set to an averaging time of 8 seconds, the second pulse oximeter is set to an averaging time of 16 seconds.

    Other: Movement artifact - knocking · Other: Movement artifact - tremor · Other: Artifact - ambient light · Other: Artifact - low perfusion · Other: SpO2 measurement

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

  • OtherSpO2 measurement

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

06

What researchers measure

Primary outcomes

  1. SpO2 readings with different averaging times

    Differences in the SpO2 signal during artifacts depending on the set averaging time.

    Time frame: 30 minutes

07

Study locations

1 site
  • Faculty of Biomedical Engineering, Czech Technical University in Prague
    Kladno, 27201, Czechia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04933773
Lead sponsor
Czech Technical University in Prague
Responsible party
Sponsor
First posted
Jun 22, 2021
Start date
May 15, 2021
Primary completion
Oct 15, 2021
Completion
Oct 15, 2021
Last update
Jan 28, 2022

Study contacts

Veronika Rafl Huttova
principal investigator · Czech Technical University in Prague

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2022. You cannot join it, but the record below documents what was studied.

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