Acébal E, Subirá S, Spatz J, Faleni R, Merzbacher B, Gales A, Moizeszowicz J
Eur J Clin Pharmacol. 1976 Jun 15;10(2):109-13. doi: 10.1007/BF00609468.
The effect of nomifensin (Hoechst 36984), a synthetic psychotropic drug whose structure differs from MAO inhibitors and tricyclics, was studied in a double blind comparative trial with desimipramine in patients with various depressive syndromes. Forty-three patients (23 in the nomifensin group and 20 in the desimipramine group) were studied for 6 weeks. Clinical follow-up was done with the Wittenborn scale (WPRS), Hamilton's rating scale for depression (HRS), Zung's scale (SDS), and the PEN inventory. The average daily dose was nomifensin 84 mg and desimipramine 76 mg. Changes in HRS, WPRS and SDS showed statistically significant improvement with both treatments. A moderate anxiolytic effect was found in the nomifensin group, whereas medication had to be discontinued in two desimipramine-treated patients because of its drive-enhancing effect. Urinary phenylethylamine excretion rose in 2 out of 8 patients after 5 weeks of treatment with nomifensin.
诺米芬辛(Hoechst 36984)是一种合成精神药物,其结构不同于单胺氧化酶抑制剂和三环类药物。在一项针对各种抑郁综合征患者的双盲对照试验中,对诺米芬辛与地昔帕明的疗效进行了研究。43名患者(诺米芬辛组23名,地昔帕明组20名)接受了为期6周的研究。采用维滕伯恩量表(WPRS)、汉密尔顿抑郁评定量表(HRS)、zung量表(SDS)和PEN问卷进行临床随访。诺米芬辛的平均日剂量为84毫克,地昔帕明为76毫克。两种治疗方法在HRS、WPRS和SDS方面的变化均显示出统计学上的显著改善。诺米芬辛组发现有中度抗焦虑作用,而两名接受地昔帕明治疗的患者因药物的增强驱力作用而不得不停药。8名患者中有2名在接受诺米芬辛治疗5周后尿苯乙胺排泄量增加。