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Expert Rev Neurother · Feb 2011
Randomized Controlled Trial Multicenter StudyEfficacy and safety of ramelteon in Japanese adults with chronic insomnia: a randomized, double-blind, placebo-controlled study.
- Naohisa Uchimura, Atsushi Ogawa, Misako Hamamura, Takamasa Hashimoto, Hiroshi Nagata, and Makoto Uchiyama.
- Department of Neuropsychiatry, Kurume University School of Medicine, Kurume, Japan.
- Expert Rev Neurother. 2011 Feb 1; 11 (2): 215-24.
AbstractThis randomized, double-blind, placebo-controlled study assessed the efficacy and safety of ramelteon 4 and 8 mg in Japanese adults with chronic insomnia. A secondary objective was to evaluate efficacy and safety when doses were uptitrated from placebo, ramelteon 4 and 8 mg to 4, 8 and 16 mg, respectively. Patient-reported sleep data were collected using sleep diaries. There was no statistically significant difference between ramelteon and placebo in the change in subjective sleep latency (sSL) in the full analysis set (n = 1130). Significant improvement was observed in the change in subjective total sleep time with ramelteon 8 mg at week 1. In post hoc analyses, ramelteon 8 mg reduced sSL in individuals with smaller fluctuations (within ±30 min) of sSL at baseline, in those with a shorter (<1 year) history of insomnia and in individuals who had not used benzodiazepines. Ramelteon up to 16 mg nightly was safe and well tolerated.
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