CClinicalTrials.gg
Status unknownNCT04660318Updated Jun 30, 2021

Assessment of Physiological Parameters Measurements (Heart Rate, Respiratory Rate, and Oxygen Saturation) by Standard Acquisition System Compared Remote Photoplethysmography Imaging System l

An interventional study of Remote photoplethysmography for physiological parameters and standard acquisition system for physiological parameters in Plethysmography, Remote Photoplethysmography Imaging and Physiological Parameters, sponsored by Central Hospital, Nancy, France. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-06-30.

Sponsored by Central Hospital, Nancy, France · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Jun 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
1,045
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

Introduced in 1930, photoplethysmography techniques presented the possibility of measuring SpO2 and HR using the absorption of light by the blood to define these signals In recent years, a new approach to photoplethysmography to measure physiological parameters without contact has been developed. This technique, called remote Photoplethysmography Imaging (rPPG), uses the different Red - Green - Blue color spectra at a skin captured by the camera video to determine a plethysmography signal.

Although these systems have been technically valid, they have not been clinically evaluated in a health setting. This clinical trial is to assess parameters measurements by rPPG compared standard acquisition system in real conditions

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Conditions studied

  • Plethysmography
  • Remote Photoplethysmography Imaging
  • Physiological Parameters
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In context

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients requiring a Pulmonary function testing.

Exclusion criteria

Exclusion Criteria:

  • Patients with stable clinical status.
  • Pregnant woman or Woman of childbearing potential without effective contraception
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,045 participants (estimated)

Study arms

  • Experimental
    Experimental: remote photoplethysmography for physiological parameters Monitor Readings

    Device: Remote photoplethysmography for physiological parameters

  • Other
    Control: rstandard acquisition system for physiological parameters Monitor Readings

    Device: standard acquisition system for physiological parameters

Interventions

  • DeviceRemote photoplethysmography for physiological parameters

    physiological parameters will be acquired using the Remote photoplethysmography software simultaneously for the conventional parameters measurements (heart rate, respiratory rate, and oxygen saturation)

  • Devicestandard acquisition system for physiological parameters

    physiological parameters will be acquired using the standard acquisition system for the conventional parameters measurements (heart rate, respiratory rate, and oxygen saturation)

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What researchers measure

Primary outcomes

  1. Concordance of rPPG heart rate readings

    Heart rateconcordance analysis by standard acquisition system (photoplethysmography of the finger) compared rPPG

    Time frame: 30-120 seconds.

  2. Concordance of rPPG respiratory rate readings

    respiratory rate concordance analysis by standard acquisition system (photoplethysmography of the finger) compared rPPG

    Time frame: 30-120 seconds.

  3. Concordance of rPPG oxygen saturation readings

    oxygen saturation concordance analysis by standard acquisition system (photoplethysmography of the finger) compared rPPG

    Time frame: 30-120 seconds.

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Study locations

1 of 1 sites recruiting
  • Centre Hospitalier Régional Universitaire de Nancy.
    Vandoeuvre les nancy, 54500, France
    Recruiting
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References and documents

Publications

  • Allado E, Poussel M, Moussu A, Saunier V, Bernard Y, Albuisson E, Chenuel B. Innovative measurement of routine physiological variables (heart rate, respiratory rate and oxygen saturation) using a remote photoplethysmography imaging system: a prospective comparative trial protocol. BMJ Open. 2021 Aug 13;11(8):e047896. doi: 10.1136/bmjopen-2020-047896. PubMed 34389569 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 30, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04660318
Lead sponsor
Central Hospital, Nancy, France
Responsible party
Sponsor
First posted
Dec 9, 2020
Start date
Dec 14, 2020
Primary completion
May 1, 2022 (estimated)
Completion
Dec 1, 2022 (estimated)
Last update
Jun 30, 2021

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jun 2021. You cannot join it, but the record below documents what was studied.

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