Wallis T D, Vallé-Jones J C, Craven J R, Hanks G W, Stonier P D
Br J Clin Pharmacol. 1979;7 Suppl 1(Suppl 1):123S-127S. doi: 10.1111/j.1365-2125.1979.tb04679.x.
1 Forty-four clinically anxious patients entered a comparative double-blind trial of clobazam 20 mg, clobazam 30 mg and dipotassium clorazepate 15 mg, all drugs given as a single dose at night. 2 Assessment by the Hamilton Anxiety Scale, Morbid Anxiety Inventory (Salkind) and a Visual Analogue Scale showed a statistically significant improvement for all treatment groups after 2 weeks, with continued improvement after a further 2 weeks. 3 Daytime drowsiness was the commonest side-effect in all treatment groups but there was a tendency for a lower incidence in patients on clobazam. There was no evidence of a dose-related incidence of drowsiness in the clobazam 20 mg and 30 mg groups. Other side-effects were few and nonspecific. 4 Clobazam is a 1,5-benzodiazepine with an elimination half-life of 18 hours. When given in single doses of 20-30 mg at night it has an equivalent effect to dipotassium clorazepate 15 mg.
44名临床焦虑患者参与了一项比较性双盲试验,试验药物为氯巴占20毫克、氯巴占30毫克和氯氮卓二钾15毫克,所有药物均在夜间单次给药。
通过汉密尔顿焦虑量表、病态焦虑量表(索尔金德)和视觉模拟量表进行评估,结果显示,所有治疗组在2周后均有统计学上的显著改善,再过2周后仍持续改善。
日间嗜睡是所有治疗组最常见的副作用,但服用氯巴占的患者发生率有较低趋势。在氯巴占20毫克和30毫克组中,没有证据表明嗜睡发生率与剂量相关。其他副作用很少且不具有特异性。
氯巴占是一种1,5 - 苯二氮䓬类药物,消除半衰期为18小时。夜间单次服用20 - 30毫克时,其效果与氯氮卓二钾15毫克相当。