Double blind controlled trials of cholecystokinin octapeptide in neuroleptic-refractory schizophrenia

Psychopharmacology (Berl). 1987;91(1):80-4. doi: 10.1007/BF00690931.

Abstract

A group of 14 schizophrenics who remained symptomatic after neuroleptic treatment received either 0.02 mcg/kg CCK-8 or saline placebo intravenously. Thereafter, 13 received the alternative infusion as a crossover treatment. A second group of 16 such patients received 0.04 mcg/kg CCK-8 or saline intravenously and, thereafter, 14 of these received the alternative infusion as a crossover treatment. Psychopathology was rated prior to, 2-3 h post, and on days 3, 5 and 7 after each infusion. Ratings consisted of the BPRS, the Abrams and Taylor Scale for Emotional Blunting, the Hamilton Anxiety Scale and a Schneiderian "Positive" symptom scale abstracted from the President State Examination. Parallel groups and cross over design analyses failed to show efficacy for CCK-8.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Antipsychotic Agents*
  • Clinical Trials as Topic
  • Double-Blind Method
  • Gastrointestinal Diseases / chemically induced
  • Humans
  • Placebos
  • Schizophrenia / drug therapy*
  • Sincalide / administration & dosage
  • Sincalide / adverse effects
  • Sincalide / therapeutic use*

Substances

  • Antipsychotic Agents
  • Placebos
  • Sincalide