Effects of zopiclone as compared to flurazepam on sleep in women over 40 years of age.

International pharmacopsychiatry Pub Date : 1982-01-01
O P Quadens, G Hoffman, G Buytaert
{"title":"Effects of zopiclone as compared to flurazepam on sleep in women over 40 years of age.","authors":"O P Quadens,&nbsp;G Hoffman,&nbsp;G Buytaert","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Zopiclone is a new nonbenzodiazepine hypnotic, the recommended dose of which is 7.5 mg. It was compared to flurazepam 30 mg in a sleep laboratory study. 12 women aged 40-60 years, with subjective sleep disorders for at least 2 months, were treated for 13 nights with each drug in a crossover double-blind design. Each active drug period was preceded by 5 days of placebo washout and followed by 35 days of withdrawal (no treatment). A baseline period of 4 nights (without treatment) was obtained before the study itself. The subjects slept in the sleep laboratory during the baseline period, during the last 3 nights on placebo, during the last 3 nights on active drug, and from the 11th to the 13th night after active drug discontinuation. Polygraphic recordings were obtained during each of these nights. The criteria of Kales and Rechtschaffen were used to score the tracings. Both drugs were shown to be effective when compared to placebo. Comparisons between the two periods with active treatment did not show significant differences for sleep onset latency, total sleep time, sleep efficiency index, stage 0, percent REM, number of REM periods, and REM latency. There was a trend towards an increase with zopiclone of the number of awakenings, percent of stage 3, percent of deep sleep, and an increase with flurazepam of the percent of light sleep. A significant difference was only found for percent of stage 2 (increased with flurazepam).</p>","PeriodicalId":75943,"journal":{"name":"International pharmacopsychiatry","volume":"17 Suppl 2 ","pages":"146-55"},"PeriodicalIF":0.0000,"publicationDate":"1982-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International pharmacopsychiatry","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Zopiclone is a new nonbenzodiazepine hypnotic, the recommended dose of which is 7.5 mg. It was compared to flurazepam 30 mg in a sleep laboratory study. 12 women aged 40-60 years, with subjective sleep disorders for at least 2 months, were treated for 13 nights with each drug in a crossover double-blind design. Each active drug period was preceded by 5 days of placebo washout and followed by 35 days of withdrawal (no treatment). A baseline period of 4 nights (without treatment) was obtained before the study itself. The subjects slept in the sleep laboratory during the baseline period, during the last 3 nights on placebo, during the last 3 nights on active drug, and from the 11th to the 13th night after active drug discontinuation. Polygraphic recordings were obtained during each of these nights. The criteria of Kales and Rechtschaffen were used to score the tracings. Both drugs were shown to be effective when compared to placebo. Comparisons between the two periods with active treatment did not show significant differences for sleep onset latency, total sleep time, sleep efficiency index, stage 0, percent REM, number of REM periods, and REM latency. There was a trend towards an increase with zopiclone of the number of awakenings, percent of stage 3, percent of deep sleep, and an increase with flurazepam of the percent of light sleep. A significant difference was only found for percent of stage 2 (increased with flurazepam).

佐匹克隆与氟拉西泮对40岁以上女性睡眠的影响
佐匹克隆是一种新的非苯二氮卓类催眠药,推荐剂量为7.5毫克。在一项睡眠实验室研究中,将其与30毫克的氟拉西泮进行了比较。12名年龄在40-60岁之间,主观性睡眠障碍至少2个月的女性,在交叉双盲设计中使用每种药物治疗13晚。每个有效药物期之前有5天安慰剂洗脱期,之后是35天停药(无治疗)。在研究开始前,基线期为4晚(未经治疗)。受试者在基线期、服用安慰剂的最后3晚、服用活性药物的最后3晚以及停用活性药物后的第11至13晚在睡眠实验室睡觉。在每一个晚上都获得了测谎记录。采用羽衣甘蓝和赤霞芬的评分标准对示踪进行评分。与安慰剂相比,这两种药物都显示出有效。在积极治疗的两个阶段之间的比较,在睡眠开始潜伏期、总睡眠时间、睡眠效率指数、0阶段、快速眼动百分比、快速眼动周期数和快速眼动潜伏期方面没有显着差异。佐匹克隆有增加觉醒次数的趋势,第三阶段的百分比,深度睡眠的百分比,氟拉西泮有增加浅睡眠的百分比。只有在第二阶段(氟西泮增加)中发现了显著的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信