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| ID | Type | Description | Link |
|---|---|---|---|
| HSP-2003-002 |
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| Name | Class |
|---|---|
| Ministry of Health, Spain | OTHER_GOV |
| REM-TAP Network | UNKNOWN |
| Pfizer | INDUSTRY |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| I ziprasidone | Active Comparator |
| |
| II placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ziprasidone | Drug | Dose flexible from 40 to 200 mg/d during 12 weeks |
| |
| Measure | Description | Time Frame |
|---|---|---|
| CGI scale for use in borderline personality disorder (CGI-BPD) | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Hamilton Rating Scale Depression (HAM-D-17) | 12 weeks | |
| Hamilton Rating Scale for Anxiety (HAM-A) | 12 weeks | |
| Brief Psychiatric Rating Scale (BPRS) |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Psychiatry, Sta. Creu and St. Pau Hospital | Barcelona | 08025 | Spain |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 36375174 | Derived | 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. | |
| 18251623 |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Jan 28, 2011 | |
| Reset | Feb 24, 2011 | |
| Release | Jan 21, 2013 | |
| Reset | Feb 22, 2013 | |
| Release | Jan 12, 2026 | |
| Reset | Jan 27, 2026 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Jan 28, 2011 | Feb 24, 2011 | |||
| Jan 21, 2013 |
| ID | Term |
|---|---|
| D001883 | Borderline Personality Disorder |
| ID | Term |
|---|---|
| D010554 | Personality Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| C092292 | ziprasidone |
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| Placebo |
| Drug |
flexible doses from 40 to 200 mg/d during 12 weeks |
|
| 12 weeks |
| SCL-90-R | 12 weeks |
| Barratt Impulsiveness Scale | 12 weeks |
| Treatment-emergent adverse events | 12 weeks |
| UKU Side Effect Rating Scale | 12 weeks |
| EKG and laboratory assessment | 12 weeks |
| Buss-Durkee Inventory | 12 weeks |
| 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. |
| Feb 22, 2013 |
| Jan 12, 2026 | Jan 27, 2026 |