Actively Recruiting

Phase Not Applicable
Age: 3Years - 17Years
All Genders
NCT06231654

Evaluation of Remote Photoplethysmography to Assist Vital Signs Measure in Pediatrics

Led by Fondation Lenval · Updated on 2026-01-28

600

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Introduced in 1930, photoplethysmography techniques presented the possibility of measuring SpO2 and heart rates (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. However, it has never been studied in pediatric patients. The objective is to evaluate the remote photoplethysmography technology to measure vital signs in pediatrics

CONDITIONS

Official Title

Evaluation of Remote Photoplethysmography to Assist Vital Signs Measure in Pediatrics

Who Can Participate

Age: 3Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged over 3 years and under 18 years
  • Any reason for consultation or hospitalization
  • Written and signed informed consent from one parent or person with parental authority
  • Membership in a social security scheme
Not Eligible

You will not qualify if you...

  • Neurocognitive disorder
  • Immediate vital distress
  • Known cardiac arrhythmia
  • Scleroderma
  • Pathological tremors or muscle spasms preventing remaining still during measurement
  • Parents who do not understand or speak French

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Fondation Lenval - Hôpitaux Pédiatriques de Nice CHU-LENVAL

Nice, France, 06200

Actively Recruiting

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Research Team

A

Antoine TRAN, MCU-MD

CONTACT

M

Marco OLLA, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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