Evaluation of L-carnitine: a double-blind comparison of L-carnitine vs. placebo in narcolepsy with cataplexy patients
Not Applicable
- Conditions
- narcolepsy with cataplexy
- Registration Number
- JPRN-UMIN000003760
- Lead Sponsor
- Yoyogi Sleep Clinic, Neuropsychiatric Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1. patients with epilepsia (including past history) 2. patients who take a acenocoumarol 3. patients with hypersensitive to components of L-carnitine and placebo 4. patients who are pregnant or desire pregnancy within this study 5. patients who participate in another clinical trial 6. doctor's judgment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of sleep diary and actigraph from 4 to 8 weeks of each administration
- Secondary Outcome Measures
Name Time Method