Treatment of tardive dyskinesia with ceruletide: a double-blind, placebo-controlled study

Psychiatry Res. 1992 Aug;43(2):129-36. doi: 10.1016/0165-1781(92)90127-o.

Abstract

The effectiveness of a once-weekly i.m. injection of ceruletide (0.8 microgram/kg) in suppressing the symptoms of neuroleptic-induced tardive dyskinesia (TD) was evaluated in a double-blind, placebo-controlled, matched-pairs study. Global evaluation of the severity of TD symptoms over the 8-week study period revealed a significant improvement with ceruletide as compared with placebo. Analysis of the therapeutic response to ceruletide over the course of treatment revealed a slow, but long-lasting improvement of TD symptoms. Side effects, which were mild and transient, consisted mainly of nausea and epigastric discomfort. The incidence of side effects did not differ between the ceruletide- and placebo-treated groups. Ceruletide appears to be a novel and practical treatment that can substantially alleviate the symptoms of dyskinesia.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Antipsychotic Agents / adverse effects*
  • Antipsychotic Agents / therapeutic use
  • Ceruletide / adverse effects
  • Ceruletide / therapeutic use*
  • Double-Blind Method
  • Dyskinesia, Drug-Induced / drug therapy*
  • Female
  • Humans
  • Male
  • Matched-Pair Analysis
  • Middle Aged
  • Neurologic Examination / drug effects
  • Schizophrenia / drug therapy*
  • Schizophrenic Psychology*

Substances

  • Antipsychotic Agents
  • Ceruletide