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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04660318
Enrollment
1045
Registered
2020-12-09
Start date
2020-12-14
Completion date
2022-12-01
Last updated
2021-06-30

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

Conditions

Physiological Parameters, Plethysmography, Remote Photoplethysmography Imaging

Brief 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

Interventions

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)

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients requiring a Pulmonary function testing.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Concordance of rPPG heart rate readings30-120 seconds.Heart rateconcordance analysis by standard acquisition system (photoplethysmography of the finger) compared rPPG
Concordance of rPPG respiratory rate readings30-120 seconds.respiratory rate concordance analysis by standard acquisition system (photoplethysmography of the finger) compared rPPG
Concordance of rPPG oxygen saturation readings30-120 seconds.oxygen saturation concordance analysis by standard acquisition system (photoplethysmography of the finger) compared rPPG

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026