Narcolepsy Trial, Recruiting NCT06336057 Sponsor: University Hospital, Toulouse Condition: Narcolepsy
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Narcolepsy Trial, Recruiting

NCT06336057
Recruiting Not Applicable

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:

For people with narcolepsy (main study group):

  • You are an adult who has been diagnosed with Type 1 narcolepsy based on recognised medical guidelines and have completed a 48-hour sleep study at a Sleep Laboratory
  • You are part of a social security system (such as having health insurance or national healthcare coverage)

For the comparison group (people without narcolepsy):

  • You are 18 years of age or older
  • You are being treated at Toulouse University Hospital for obstructive sleep apnea (a condition where breathing repeatedly stops during sleep) and your treatment is working well, showing little to no remaining sleep apnea
  • You are part of a social security system (such as having health insurance or national healthcare coverage)

Who may not be able to join:

  • You have a history of autism spectrum disorder, a long-term psychotic disorder, or bipolar disorder
  • You have a history of memory or thinking difficulties caused by a neurological condition (a condition affecting the brain or nervous system)
  • Your level of French language understanding is not sufficient to complete the study questionnaires
  • You are currently under a legal protection measure, guardianship, or curatorship (a formal arrangement where someone else manages your affairs)
  • You are currently 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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Rachel DEBS, MD, Centre de compétence Narcolepsies et Hypersomnies rares, CHU de Toulouse, Hôpital Pierre-Paul Riquet

Phone: 05 61 77 94 88

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

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
17 May 2024
Est. completion
17 May 2024

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Comparison of mentalization abilities, in a population of patients with NT1 versus a control group.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov