Gachoud J P, Dick P, Köhler M
Roche Pharma (Schweiz) AG, Reinach.
Clin Neuropharmacol. 1994;17 Suppl 1:S29-37. doi: 10.1097/00002826-199417001-00005.
We report the results of a multicenter, double-blind study conducted in a general practice setting, in which the efficacy and tolerability of moclobemide, a new antidepressant drug of the reversible inhibitor of monoamine oxidase type A class, were compared with those of maprotiline, a noradrenaline reuptake inhibitor often prescribed in the general practice setting. Participating general practitioners were required to make differential diagnoses of depressive disorders according to DSM-III criteria and then quantitatively assess the efficacy of treatment using the Hamilton Depression Rating Scale (HDRS) and the Zung self-rating depression scale (Zung SDS). One hundred thirty outpatients (mean age 48 years) with major depression according to DSM-III were randomized to receive either moclobemide 300 mg or maprotiline 75 mg daily for 4 weeks. From day 8, dosages were increased if necessary up to a maximum of 400 mg of moclobemide or 100 mg of maprotiline. The results showed that moclobemide was as effective as maprotiline (HDRS, Zung SDS); moclobemide appeared to have the same antidepressant and anxiolytic activity, but a stronger drive-enhancing effect. Moclobemide was the better-tolerated drug, producing fewer side effects than maprotiline did: in particular, fewer instances of somnolence and dry mouth. The good tolerability of the compound was confirmed by the qualitative assessments of the study physicians.
我们报告了一项在普通医疗环境中进行的多中心、双盲研究的结果,该研究将新型抗抑郁药物A类单胺氧化酶可逆抑制剂吗氯贝胺的疗效和耐受性,与普通医疗环境中常用的去甲肾上腺素再摄取抑制剂马普替林进行了比较。参与研究的全科医生需根据《精神疾病诊断与统计手册》第三版(DSM-III)标准对抑郁症进行鉴别诊断,然后使用汉密尔顿抑郁量表(HDRS)和zung自评抑郁量表(Zung SDS)对治疗效果进行定量评估。130名符合DSM-III标准的重度抑郁症门诊患者(平均年龄48岁)被随机分为两组,一组每天服用300毫克吗氯贝胺,另一组每天服用75毫克马普替林,为期4周。从第8天起,必要时可增加剂量,吗氯贝胺最大剂量为400毫克,马普替林最大剂量为100毫克。结果显示,吗氯贝胺与马普替林疗效相当(HDRS、Zung SDS);吗氯贝胺似乎具有相同的抗抑郁和抗焦虑活性,但具有更强的促动力作用。吗氯贝胺是耐受性更好的药物,产生的副作用比马普替林少:尤其是嗜睡和口干的情况较少。研究医生的定性评估证实了该化合物的良好耐受性。