Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 years or older
- People who have been diagnosed with obstructive sleep apnea (a condition where breathing repeatedly stops during sleep) with a severity score of 5 or more on a standard sleep test, and whose condition requires CPAP treatment (a breathing machine used during sleep)
Who may not be able to join:
- People whose sleep apnea is caused by a neurological (brain or nervous system) condition, or is a mixed type (confirm with trial site)
- People for whom CPAP treatment is not medically suitable, or who do not wish to use it
- People who have cognitive disorders (conditions affecting memory, thinking, or understanding)
- People who are under legal guardianship or curatorship (where another person has been appointed to make decisions on their behalf)
- People who are under court-ordered legal protection
- People who are not registered with a social security scheme (confirm with trial site regarding what this means in your country)
- Women who are pregnant or currently breastfeeding
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Marie DEVAUX, Dr, CHU d'Orléans
Phone: +332 38 74 40 71
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in Daytime sleepiness
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.