Plasma levels and therapeutic response with trimipramine treatment of endogenous depression

J Clin Psychiatry. 1988 Mar;49(3):113-6.

Abstract

In a 6-week, double-blind study involving 34 endogenously depressed patients, plasma trimipramine levels of two dosage groups, 75-mg/day and 150-mg/day, were compared with regard to clinical efficacy as determined by scores on the Hamilton Rating Scale for Depression, the Clinical Global Impressions scale, and the Zung Self-Rating Depression Scale. Both dosage levels of trimipramine produced prompt, consistent, and progressive antidepressant effects. No correlation between plasma levels and clinical efficacy was found.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Adult
  • Clinical Trials as Topic
  • Depressive Disorder / drug therapy*
  • Depressive Disorder / psychology
  • Dibenzazepines / blood*
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Middle Aged
  • Psychiatric Status Rating Scales
  • Random Allocation
  • Sleep Stages
  • Trimipramine / administration & dosage
  • Trimipramine / adverse effects
  • Trimipramine / blood*
  • Xerostomia / chemically induced

Substances

  • Dibenzazepines
  • Trimipramine