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A controlled trial of oxypertine in tardive dyskinesia.

Abstract
A study was undertaken to investigate the effects of oxypertine in treating tardive dyskinesia. The design was double-blind, placebo-controlled, between-patient, in 28 patients from whom previous medication was withdrawn, with 14 patients in each group. Treatment was for 4 weeks. Although more oxypertine patients improved than placebo, i.e. 71.4 vs. 50%, the results did not reach statistically significant difference. A further study is planned to increase the overall number of patients in the study, and to lengthen treatment periods.
AuthorsH L Freeman, S D Soni, L Carpenter
JournalInternational pharmacopsychiatry (Int Pharmacopsychiatry) Vol. 15 Issue 5 Pg. 281-91 ( 1980) ISSN: 0020-8272 [Print] Switzerland
PMID6114934 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Antipsychotic Agents
  • Indoles
  • Piperazines
  • Dopamine
Topics
  • Adolescent
  • Adult
  • Aged
  • Antipsychotic Agents (adverse effects)
  • Clinical Trials as Topic
  • Dopamine (metabolism)
  • Double-Blind Method
  • Dyskinesia, Drug-Induced (drug therapy)
  • Female
  • Humans
  • Indoles (therapeutic use)
  • Male
  • Middle Aged
  • Piperazines (therapeutic use)
  • Time Factors

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