Actively Recruiting

Phase Not Applicable
Age: 1Year - 20Years
All Genders
NCT04971850

Sleep-disordered Breathing and Neurocognitive Assessment in Children and Young Adults

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-04-03

1200

Participants Needed

1

Research Sites

312 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

U

URC-CIC Paris Descartes Necker Cochin

Collaborating Sponsor

AI-Summary

What this Trial Is About

One of main problems in the management of sleep-disordered breathing (SDB) in children and young adults is their screening, and the absence or the weak correlation between clinical symptoms and polysomnography (PSG). It may be useful to use additional measures together with PSG to improve the detection and characterization of respiratory events during sleep and/or correlation with clinical signs of SDB. The primary objective of the study is to determine whether psychological and neuropsychological test scores correlate with diagnostic PSG results.

CONDITIONS

Official Title

Sleep-disordered Breathing and Neurocognitive Assessment in Children and Young Adults

Who Can Participate

Age: 1Year - 20Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 1 to 20 years with suspicion or high risk of sleep-disordered breathing
  • Hospitalized at Necker Hospital for a sleep study
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • No social insurance
  • Significant psychomotor retardation
  • Unable to cooperate
  • Significant agitation
  • Acute condition or temporary drug treatments interfering with PSG results
  • Patient under guardianship or curatorship

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

Hôpital Necker-Enfants Malades

Paris, France, 75015

Actively Recruiting

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Research Team

B

Brigitte Fauroux, MD, PhD

CONTACT

H

Hélène Morel

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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