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
- Men or women
- People who have signed a free and informed consent form
- People who are part of a social protection scheme (such as health insurance or social security coverage)
- People in one of the following groups: those with a primary sleep-wake disorder; those with a neurological condition that affects sleep and wakefulness; those with a psychiatric condition that affects sleep and wakefulness; those with an eye condition that may affect how light is received or processed by the eye; those with light sensitivity that affects sleep and wake regulation; or healthy individuals with no relevant conditions
Who may not be able to join:
- People with Age-Related Macular Degeneration (AMD) or similar conditions affecting the retina, such as retinitis pigmentosa or diabetes-related damage to the eye
- People with cataracts that have caused significant vision loss (below 5/10 vision)
- People with abnormal blood vessel growth behind the retina (confirm with trial site)
- People who are currently in an exclusion period due to participation in another study
- People for whom it is not possible to provide proper informed consent, such as those in an emergency situation or those who have difficulty understanding the information
- People who are under the protection of the justice system
- People who are under guardianship or supervised legal protection
- People who are pregnant or 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: Bourgin Patrice, MD, University Hospital, Strasbourg, France
Phone: 03 88 11 64 30
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
PIPR : Post-Illumination Pupil Response
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.