Clin2
NCT05837091Possibly a fitRecruiting

Low-dose sodium oxybate for idiopathic hypersomnia sleepiness

Idiopathic Hypersomnia

Treatments studied

Part of Brain & nervous system, Mental health clinical trials.

This trial tests whether low-dose sodium oxybate can improve symptoms in adults with idiopathic hypersomnia, a condition that causes excessive sleepiness. You’d likely be asked to pause this standard treatment briefly while baseline testing is completed, and you’d use reliable contraception during and after the study drug.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
30 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You are 18–65 years old and have a primary diagnosis of idiopathic hypersomnia (IH) that fits the study’s sleep-disorder criteria
  • Your body mass index (BMI) is between 18 and 35
  • Most days you sleep at least 9 hours (including naps), based on at least 10 of 14 days of a sleep diary
  • You score at least 10 on the Epworth Sleepiness Scale (done at pre-screening)
  • A sleep specialist has recommended low-dose sodium oxybate (LSO) as part of usual care, and you agree to delay it until baseline tests are finished
  • If you take wake-promoting medicines or antidepressants, your dose must be stable for at least 2 months before starting and stay stable during the main study

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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