Pharmacopsychiatry 2008; 41(6): 232-239
DOI: 10.1055/s-0028-1082072
Original Paper

© Georg Thieme Verlag KG Stuttgart · New York

A Double-blind Placebo-controlled Discontinuation Study of Zuclopenthixol for the Treatment of Aggressive Disruptive Behaviours in Adults with Mental Retardation – Secondary Parameter Analyses

F. Häßler 1 , T. Glaser 2 , A. F. Pap 2 , M. Beneke 2 , A. Diefenbacher 3 , O. Reis 1 and the Zuclopenthixol Disruptive Behaviour Study Group
  • 1Clinic for Child and Adolescent Psychiatry, University of Rostock, Rostock, Germany
  • 2Bayer Vital GmbH, Leverkusen, Germany
  • 3Clinic for Psychiatry, Psychotherapy and Psychosomatics, Queen Elisabeth Hospital, Herzberge, Berlin, Germany
Weitere Informationen

Publikationsverlauf

received 13.12.2007 revised 21.04.2008

accepted 25.04.2008

Publikationsdatum:
09. Dezember 2008 (online)

Preview

Abstract

Introduction: Earlier studies showed risperidone to be effective in the treatment of aggression and self-injurious behaviour in adults with mental retardation but also having adverse side effects. This study was conducted to evaluate the effects of zuclopenthixol withdrawal.

Methods: After open treatment with zuclopenthixol (n=49) responders were randomly assigned to continue (n=19) or discontinue (n=20) zuclopenthixol treatment during a 12-week double-blind, placebo-controlled period. Effects were measured using the Disability Assessment Schedule (DAS), improvement on the Clinical Global Impression Scale (CGI-I), and the Nurse's Observation Scale for Inpatient Evaluation (NOSIE).

Results: Ten patients (20%) discontinued the study due to insufficient therapeutic effect or adverse events in the open period. Efficacy: The superiority of zuclopenthixol over placebo among all randomized patients was supported not only by primary efficacy measure but also by the comparisons of mean scores of all secondary efficacy measures tested in a step-down-procedure (DAS, p<0.001; CGI-I, p<0.002, NOSIE, p<0.005). Safety: In both groups, one patient discontinued (5%) for adverse events. Adverse events were generally mild or moderate in severity.

Discussion: Zuclopenthixol proved to be safe and effective to keep a low rate of aggressive behaviour in adults with mental retardation.

References

Correspondence

F. Häßler

Clinic for Child and Adolescent Psychiatry

University of Rostock

Gehlsheimer Straße 20

18147 Rostock

Germany

Telefon: +49/381/494 46 00

Fax: +49/381/494 46 02

eMail: frank.haessler@med.uni-rostock.de