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 (BPD). Method: Sixty BPD patients were included 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 two-week baseline period. The Clinical Global Impression scale for use in BPD 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.
The American Psychiatric Association (APA) Guidelines for the Treatment of Borderline personality disorder recommend that pharmacological treatment for BPD has an important adjunctive role, especially for diminution of symptoms such as affective instability, impulsivity, psychotic-like symptoms, and self-destructive behavior. Studies conducted with low doses of conventional antipsychotics have showed significant improvements in specific symptoms such as hostility, impulsiveness, mood, and psychotic symptoms. The introduction of atypical antipsychotics, with a more favorable tolerance profile, increases clinicians' options for treating BPD. Olanzapine has proven its efficacy in four double-blind, placebo-controlled clinical trials in patients with BPD. Ziprasidone is an atypical antipsychotic with a pharmacological action on serotonergic, dopaminergic and adrenergic receptors. It has proven to be effective for schizophrenia, schizoaffective and acute mania disorders and the incidence of side effects is low. Although clinical findings and the pharmacological activity of ziprasidone suggest the drug may have therapeutic benefits in BPD patients, no controlled studies have yet been conducted in these patients. We carried out a randomized, double-blind, placebo-controlled study to evaluate efficacy and tolerability of ziprasidone in the management of BPD patients with moderate-high clinical severity.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
60
Dose flexible from 40 to 200 mg/d during 12 weeks
flexible doses from 40 to 200 mg/d during 12 weeks
Department of Psychiatry, Sta. Creu and St. Pau Hospital
Barcelona, Spain
CGI scale for use in borderline personality disorder (CGI-BPD)
Time frame: 12 weeks
Hamilton Rating Scale Depression (HAM-D-17)
Time frame: 12 weeks
Hamilton Rating Scale for Anxiety (HAM-A)
Time frame: 12 weeks
Brief Psychiatric Rating Scale (BPRS)
Time frame: 12 weeks
SCL-90-R
Time frame: 12 weeks
Barratt Impulsiveness Scale
Time frame: 12 weeks
Treatment-emergent adverse events
Time frame: 12 weeks
UKU Side Effect Rating Scale
Time frame: 12 weeks
EKG and laboratory assessment
Time frame: 12 weeks
Buss-Durkee Inventory
Time frame: 12 weeks
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