Analyzing body fluids in narcolepsy patients
Official title: Proteomics and Metabolomics of Body Fluid in Patients With Narcolepsy
Run by Qilu Hospital of Shandong University · NCT06279247 · Data updated 2026-11-12
This study looks at body fluids from people with narcolepsy and healthy volunteers to see if there are any unique markers that could help better understand the condition.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 5 Years to 100 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Qilu Hospital of Shandong University Academic / other |
| Locations | 1 site (Jinan, Shandong) |
| Status | Recruiting |
| Started | September 1, 2022 |
| Main results expected | August 26, 2026 |
| Study ends | August 26, 2027 |
| Registry record updated | March 24, 2026 |
| Trial ID | NCT06279247 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include individuals diagnosed with narcolepsy type 1 or type 2 according to the International Classification of Sleep Disorders.
✕Probably not a fit
Patients with primary hypersomnia, other sleep disorders, or significant comorbidities may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study focuses on the proteomics and metabolomics of body fluids in patients with narcolepsy, comparing them to healthy volunteers. It aims to identify potential molecular markers associated with narcolepsy by analyzing blood, urine, stool, and cerebrospinal fluid samples. The study will assess various factors, including sleepiness and sleep quality, using established scales. By understanding the biochemical differences, the research seeks to shed light on the pathogenesis of narcolepsy and improve diagnostic accuracy.
Why it matters
Potential benefit: If successful, this study could lead to better diagnostic tools and treatment strategies for narcolepsy patients.
How similar studies have gone: While the approach of using proteomics and metabolomics in narcolepsy is relatively novel, similar methodologies have shown promise in other neurological conditions.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria * All patients met the diagnostic criteria of the International Classification of Sleep Disorders, Third edition (ICSD-3). Exclusion Criteria * primary hypersomnia or hypersomnia due to shift work, sleep deprivation and other sleep rhythm disturbances; * excessive sleep due to drug abuse; * suffering from Parkinson's disease, Alzheimer's disease and other nervous system diseases and mental diseases; * complicated with heart, lung, liver, kidney, blood endocrine system and other basic diseases, or acute chronic infection in a short period of time; * Use of sedatives, hypnotics, antidepressants, lithium and dopamine receptor antagonists for two weeks before examination; * patients who cannot cooperate with PSG and MSLT due to various factors.
Where it's running
-
Qilu Hospital of Shandong University
Jinan, Shandong, China Recruiting
Study contacts
- Study coordinator: haiyun li
- Email: haiyunli1122@163.com
- Phone: 18560088921
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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HBS-301 for Narcolepsy: daily wakefulness and sleepiness improvement in adults
This Phase 3 study tests HBS-301 vs placebo in adults with narcolepsy to see if it helps with daytime sleepiness, cataplexy, sleepiness, and fatigue.
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Expanded-dosing Xywav vs placebo in narcolepsy and IH
This study tests whether expanded nightly dosing of Xywav helps adults with narcolepsy or idiopathic hypersomnia, compared with placebo.
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Testing Lu AH69593 for safety and tolerance in healthy adults and people with narcolepsy
This study tests whether Lu AH69593 is safe and well tolerated in adults, including those with narcolepsy, and looks at how the body processes the drug with and without food.
-
Samelisant for Narcolepsy: A Phase 3 Test for EDS and Cataplexy
This phase 3 study tests whether Samelisant can reduce daytime sleepiness and cataplexy in adults with narcolepsy.
-
E2086 for adults with narcolepsy: find the best dose compared with placebo
This study tests different doses of E2086 against placebo in adults with narcolepsy to see if it reduces daytime sleepiness.
-
Exploring the effects of light and electrical stimulation on sleep disorders
This study is testing if light therapy and brain stimulation can help people with sleep disorders like insomnia and narcolepsy get better sleep.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.