Abstract | BACKGROUND: To assess the effectiveness and safety of modafinil vs. no active treatment or other drugs in the treatment of narcolepsy. MATERIAL/METHODS: The following electronic databases were searched throughout January 2009: MEDLINE, EMBASE and The Cochrane Library. Additional references were obtained from reviewed articles. Only randomized controlled trials were included. RESULTS: We included 9 trials involving 1,054 patients in the study. Modafinil in comparison with placebo brings significant benefit in terms of elimination of excessive daytime sleepiness assessed by: ESS scale--weighted mean difference (WMD) -2.73 points (95%CI -3.39, -2.08), MSLT test--WMD 1.11 minutes (95%CI 0.55, 1.66) and MWT test--WMD 2.82 minutes (95%CI 2.40, 3.24), as well as the number and duration of somnolence, sleep attacks and naps per day, but was not different from placebo in the number of attacks of cataplexy per day. Modafinil in comparison with placebo improved quality of life of narcoleptic patients according to SF-36 questionnaire, but was associated with more common nausea. It had similar effect on excessive daytime sleepiness as sodium oxybate and was associated with less common nausea. CONCLUSIONS:
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Authors | Dominik Golicki, Malgorzata M Bala, Maciej Niewada, Aleksandra Wierzbicka |
Journal | Medical science monitor : international medical journal of experimental and clinical research
(Med Sci Monit)
Vol. 16
Issue 8
Pg. RA177-86
(Aug 2010)
ISSN: 1643-3750 [Electronic] United States |
PMID | 20671626
(Publication Type: Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't, Review, Systematic Review)
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Chemical References |
- Benzhydryl Compounds
- Neuroprotective Agents
- Placebos
- Modafinil
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Topics |
- Adolescent
- Adult
- Aged
- Benzhydryl Compounds
(adverse effects, therapeutic use)
- Female
- Humans
- Male
- Middle Aged
- Modafinil
- Narcolepsy
(drug therapy)
- Neuroprotective Agents
(adverse effects, therapeutic use)
- Placebos
- Treatment Outcome
- Young Adult
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