Lôo H, Guelfi J D, Malka R, Brion S, Cottin M, Gailledreau J, Raab A, Salfati M, Sarda A, Godchau M
Encephale. 1986 Sep-Oct;12(5):291-7.
The anxiolytic efficacy of tetrabamate was evaluated in 68 out-patients presenting an anxiety state with alcohol abuse according to DSM III criteria. The study followed a double-blind placebo-controlled design with parallel groups and lasted for 21 days. Anxiety was evaluated by the Hamilton anxiety scale, Norris visual analog scales, and the Hopkins Symptom Check List, along with the investigator's assessment. Safety was evaluated in terms of somatic symptoms (CHESS 84) and the physician's overall evaluation. The anxiolytic activity of tetrabamate (three 300 mg tablets/day) was significantly greater than that of placebo from seventh day on. There were no statistically significant differences in safety profile between tetrabamate and placebo. Moreover, in the tetrabamate group the significantly greater improvement in the scores of somatic symptoms indicates that the compound caused no notable adverse effects and its activity on somatic complaints (psychopathologic and/or toxic).
根据《精神疾病诊断与统计手册》第三版标准,对68名患有焦虑症且有酒精滥用问题的门诊患者评估了四甲铵的抗焦虑疗效。该研究采用双盲安慰剂对照平行组设计,持续21天。通过汉密尔顿焦虑量表、诺里斯视觉模拟量表、霍普金斯症状清单以及研究者的评估来评估焦虑情况。从躯体症状(CHESS 84)和医生的总体评估方面评估安全性。从第7天起,四甲铵(每日三片300毫克片剂)的抗焦虑活性显著高于安慰剂。四甲铵和安慰剂在安全性方面无统计学显著差异。此外,在四甲铵组中,躯体症状评分的显著更大改善表明该化合物未引起明显不良反应,且其对躯体主诉(精神病理和/或毒性)有活性。