Ziprasidone in the Treatment of Borderline Personality Disorder: A Double-Blind, Placebo-Controlled, Randomized Study

Juan Carlos Pascual, MD; Joaquim Soler, PsyD; Dolors Puigdemont, MD; Rosario Pérez-Egea, MD; Thais Tiana, PsyD; Enrique Alvarez, MD, PhD; and Ví­ctor Pérez, MD, PhD

Published: March 18, 2008

Article Abstract

Objective: The aim of this double-blind, placebo-controlled study was to evaluate the efficacy and tolerability of ziprasidone in the treatment of adult patients with borderline personality disorder.

Method: Sixty DSM-IV borderline personality disorder patients were included from March 2004 to April 2006 in a 12-week, single-center, double-blind, placebo-controlled study. The subjects were randomly assigned to ziprasidone or placebo in a 1:1 ratio following a 2-week baseline period. The Clinical Global Impressions scale for use in borderline personality disorder patients (CGI-BPD) was the primary outcome measure, and other scales and self-reports related to affect, behavior, psychosis, general psychopathology domains, and clinical safety were included.

Results: Analysis of variance indicated no statistically significant differences between ziprasidone and placebo in the CGI-BPD. Nor were significant differences observed between groups in depressive, anxiety, psychotic, or impulsive symptoms. The mean daily dose of ziprasidone was 84.1 mg/day (SD = 54.8; range, 40-200). The drug was seen to be safe, and no serious adverse effects were observed.

Conclusion: This trial failed to show a significant effect of ziprasidone in patients with borderline personality disorder.

Trial Registration: clinical Identifier: NCT00635921

Volume: 69

Quick Links: Personality Disorders

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