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Ziprasidone in the Treatment of Borderline Personality Disorder

Primary Purpose

Borderline Personality Disorder

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
ziprasidone
Placebo
Sponsored by
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Borderline Personality Disorder focused on measuring Borderline Personality Disorder, ziprasidone

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • DSM-IV diagnosis of Borderline Personality Disorder
  • Age between 18 and 45 years
  • Clinical Global Impression of Severity (CGI-S)scores >4

Exclusion Criteria:

  • No comorbidity with schizophrenia, drug-induced psychosis, organic brain syndrome, alcohol or other substance dependence, bipolar disorder, mental retardation, or major depressive episode in course
  • current use of medically accepted contraception in the case of female patients.

Sites / Locations

  • Department of Psychiatry, Sta. Creu and St. Pau Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

I ziprasidone

II placebo

Arm Description

Outcomes

Primary Outcome Measures

CGI scale for use in borderline personality disorder (CGI-BPD)

Secondary Outcome Measures

Hamilton Rating Scale Depression (HAM-D-17)
Hamilton Rating Scale for Anxiety (HAM-A)
Brief Psychiatric Rating Scale (BPRS)
SCL-90-R
Barratt Impulsiveness Scale
Treatment-emergent adverse events
UKU Side Effect Rating Scale
EKG and laboratory assessment
Buss-Durkee Inventory

Full Information

First Posted
March 11, 2008
Last Updated
March 11, 2008
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Collaborators
Ministry of Health, Spain, REM-TAP Network, Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT00635921
Brief Title
Ziprasidone in the Treatment of Borderline Personality Disorder
Official Title
Ziprasidone in the Treatment of Borderline Personality Disorder: A Double-Blind, Placebo-Controlled, Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2008
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
April 2006 (Actual)
Study Completion Date
April 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Collaborators
Ministry of Health, Spain, REM-TAP Network, Pfizer

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Borderline Personality Disorder
Keywords
Borderline Personality Disorder, ziprasidone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
I ziprasidone
Arm Type
Active Comparator
Arm Title
II placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
ziprasidone
Intervention Description
Dose flexible from 40 to 200 mg/d during 12 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
flexible doses from 40 to 200 mg/d during 12 weeks
Primary Outcome Measure Information:
Title
CGI scale for use in borderline personality disorder (CGI-BPD)
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Hamilton Rating Scale Depression (HAM-D-17)
Time Frame
12 weeks
Title
Hamilton Rating Scale for Anxiety (HAM-A)
Time Frame
12 weeks
Title
Brief Psychiatric Rating Scale (BPRS)
Time Frame
12 weeks
Title
SCL-90-R
Time Frame
12 weeks
Title
Barratt Impulsiveness Scale
Time Frame
12 weeks
Title
Treatment-emergent adverse events
Time Frame
12 weeks
Title
UKU Side Effect Rating Scale
Time Frame
12 weeks
Title
EKG and laboratory assessment
Time Frame
12 weeks
Title
Buss-Durkee Inventory
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: DSM-IV diagnosis of Borderline Personality Disorder Age between 18 and 45 years Clinical Global Impression of Severity (CGI-S)scores >4 Exclusion Criteria: No comorbidity with schizophrenia, drug-induced psychosis, organic brain syndrome, alcohol or other substance dependence, bipolar disorder, mental retardation, or major depressive episode in course current use of medically accepted contraception in the case of female patients.
Facility Information:
Facility Name
Department of Psychiatry, Sta. Creu and St. Pau Hospital
City
Barcelona.
ZIP/Postal Code
08025
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
36375174
Citation
Stoffers-Winterling JM, Storebo OJ, Pereira Ribeiro J, Kongerslev MT, Vollm BA, Mattivi JT, Faltinsen E, Todorovac A, Jorgensen MS, Callesen HE, Sales CP, Schaug JP, Simonsen E, Lieb K. Pharmacological interventions for people with borderline personality disorder. Cochrane Database Syst Rev. 2022 Nov 14;11(11):CD012956. doi: 10.1002/14651858.CD012956.pub2.
Results Reference
derived
PubMed Identifier
18251623
Citation
Pascual JC, Soler J, Puigdemont D, Perez-Egea R, Tiana T, Alvarez E, Perez V. Ziprasidone in the treatment of borderline personality disorder: a double-blind, placebo-controlled, randomized study. J Clin Psychiatry. 2008 Apr;69(4):603-8. doi: 10.4088/jcp.v69n0412.
Results Reference
derived

Learn more about this trial

Ziprasidone in the Treatment of Borderline Personality Disorder

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