Pecknold J C, Ban T A, Lehmann H E, Klingner A
Int J Clin Pharmacol Biopharm. 1975 Jun;11(4):304-8.
An uncontrolled clinical trial with 10 depressed patients was conducted to identify the psychopathological symptoms which may be affected by nomifensin administration, and to reveal the possible adverse effects of the drug. Consistent statistically significant improvement was noted in the course of the clinical trial on all of the assessment instruments used, and - with the exception of one patient - all improved while receiving nomifensin. Most of the therapeutic changes were seen within the first three weeks of treatment, and they included improvements of depression, as well as of hostility, a symptom which usually remains unaffeCTED BY TRICYclic antidepressant drugs. To verify the favorable therapeutic effects of nomifensin in depressed psychiatric patients, a standard-controlled clinical trial is in progress; and to verify the action mechanism of nomifensin, a study employing the probenecid technique and the measurement of spinal homovanillic acid (HVA) and 5-hydroxyindole acetic acid (5hiaa) concentration is planned.
对10名抑郁症患者进行了一项非对照临床试验,以确定可能受诺米芬辛给药影响的精神病理症状,并揭示该药物可能的不良反应。在临床试验过程中,所用的所有评估工具均显示出具有统计学意义的持续改善,并且除一名患者外,所有患者在接受诺米芬辛治疗时均有改善。大多数治疗变化出现在治疗的前三周内,包括抑郁症状以及敌意症状的改善,而敌意症状通常不受三环类抗抑郁药影响。为了验证诺米芬辛对抑郁症精神病患者的良好治疗效果,一项标准对照临床试验正在进行中;为了验证诺米芬辛的作用机制,计划开展一项采用丙磺舒技术以及测量脊髓高香草酸(HVA)和5-羟吲哚乙酸(5HIAA)浓度的研究。