Efficacy and Safety of Doxepin 1 mg, 3 mg, and 6 mg in Elderly Patients With Primary Insomnia: A Randomized, Double-Blind, Placebo-Controlled Crossover Study

被引:72
|
作者
Scharf, Martin [1 ]
Rogowski, Roberta [2 ]
Hull, Steven [3 ,4 ]
Cohn, Martin [5 ]
Mayleben, David [6 ]
Feldman, Neil [7 ]
Ereshefsky, Larry [8 ]
Lankford, Alan [9 ]
Roth, Thomas [10 ]
机构
[1] Tristate Sleep Disorders Ctr, Cincinnati, OH 45246 USA
[2] Somaxon Pharmaceut Inc, San Diego, CA USA
[3] Vince & Associates Clin Rcs, Overland Pk, KS USA
[4] SomniTech Inc, Overland Pk, KS USA
[5] Sleep Disorders Ctr SW Florida, Naples, Italy
[6] Res Management Associates, Cincinnati, OH USA
[7] St Petersburg Sleep Disorders Ctr, St Petersburg, FL USA
[8] Calif Clin Trials, Glendale, CA USA
[9] Sleep Disorders Ctr Georgia, Atlanta, GA USA
[10] Henry Ford Hosp Sleep Ctr, Detroit, MI USA
关键词
D O I
10.4088/JCP.v69n1005
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objectives: Evaluate efficacy and safety of the histamine-H, antagonist doxepin at doses of 1mg, 3 mg, and 6 mg in elderly adults with primary insomnia, Design: A randomized, double-blind, placebo-controlled. crossover design Was used in this population of elderly adults with primary insomnia (DSM-IV). Each treatment period consisted of 2 polysomnouraphic (PSG) assessment nights with a 5- or 12-day drug-free interval between periods. The study was conducted from September 2004 to January 2005. Setting: Sleep laboratories in 11 sleep centers in the United States. Participants: Elderly adults with primary insomnia. Intervention: Doxepin 1 mg, 3 mg, and 6 mg. Measurements: Efficacy was assessed using PSG and patient-reported measures. Results: Seventy-six patients were randomly assigned. All 3 doxepin closes produced dose-related significant improvements in PSG-determined wake time during sleep (p < .0001), wake time after sleep onset (p < .0001), total sleep time (p < .0001), and overall sleep efficiency (p < .0001) versus placebo. At the 3-mg and 6-mg doses, sleep efficiency was significantly improved during all thirds of the night (p < .05) There was a dose-related decrease in patient-reported sleep latency, with the 6-mg dose achieving statistical significance in latency to sleep onset (p = .0181). The pattern of the remaining subjective efficacy results was consistent with PSG. All 3 doxepin (loses had side effect profiles comparable to placebo, with no spontaneously reported anticholinergic effects, no memory impairment, and no significant next-day residual effects. Conclusions: In this 2-night study of elderly adults with primary insomnia, doxepin doses of 1 mg, 3 mg, and 6 mg were well tolerated and produced significant improvement in objective and subjective sleep maintenance and duration endpoints that persisted into the final hour of the night. Positive effects on patient-reported sleep onset were observed at the highest dose. All 3 doxepin doses had a safety profile comparable to placebo. These data demonstrate that doxepin was efficacious in improving sleep in elderly adults. (J Clin Psychiatry 2008;69:1557-1564)
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收藏
页码:1557 / 1564
页数:8
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