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OpenTrials
Completed

NCT Number: NCT06898008

Characterization of Children with Complaints of Excessive Daytime Sleepiness

10% of the population suffers from excessive daytime sleepiness. This can be explained by a variety of etiologies: psychiatric disorders, altered sleep quantity or quality, hypersomnia... The consequences on quality of life are not negligible, with emotional, academic, social, financial and somatic repercussions. Diagnosing and managing them is essential. This is the role of the HFME's Child Sleep Service, a reference center for rare narcolepsy and hypersomnia, which carries out a weekly hypersomnia assessment. In this context, the investigators are carrying out a retrospective descriptive study, the primary objective of which is to describe the results and diagnoses of hypersomnia check-ups in the HFME's Sleep Department, in order to obtain feedback on the center's activity and its evolution.

The secondary objectives are to characterize the patients in the different diagnostic groups, to highlight factors associated with the different diagnoses, and to describe changes in patient characteristics over time.

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Service d'épileptologie clinique, des troubles du sommeil et de neurologie fonctionnelle de l'enfant - Hôpital Femme Mère Enfant

France, Bron, 69500

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Patient hospitalized in the HFME sleep department for a "diagnostic assessment of hypersomnia".
  • Age under 18 at the time of hospitalization
  • From January 2015 to December 2023

Exclusion criteria

  • - No balance sheet
  • Age over 18 at time of hospitalization
  • Assessment for medicolegal or therapeutic adaptation purposes

Treatment and study plan

Assessment of socio-demographic, anthropometric, psychometric and clinical characteristics

Other

age, sex and place of residence, socioeconomic level, education, anthropometric data, first-degree family history, screen time, physical activity time, sleep time, comorbidity, drug treatments, education, total IQ, results of Epworth, CDI, ISI, ADHD, CONNERS, SCSC, Horne and Ostberg questionnaires, hearing aids, referring professional, melatonin dosage, ferritinemia, etiology of sleepiness

Primary outcomes

  1. Describe the results and diagnoses of hypersomnia assessments in the HFME Sleep Department

    Time frame: Feedback consultation 1 month after inpatient assessment

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Acronym: CEPSDE

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Mar 27, 2025
Registry last updated
Mar 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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