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Article: The clinical effectiveness and cost effectiveness of clozapine for inpatients with severe borderline personality disorder (CALMED study): a randomised placebo-controlled trial.

Crawford, Mike J / Leeson, Verity C / Evans, Rachel / Barrett, Barbara / McQuaid, Aisling / Cheshire, Jack / Sanatinia, Rahil / Lamph, Gary / Sen, Piyal / Anagnostakis, Katina / Millard, Louise / Qurashi, Inti / Larkin, Fintan / Husain, Nusrat / Moran, Paul / Barnes, Thomas R E / Paton, Carol / Hoare, Zoe / Picchioni, Marco /
Gibbon, Simon

Therapeutic advances in psychopharmacology

2022  Volume 12, Page(s) 20451253221090832

Abstract: Background: Data from case series suggest that clozapine may benefit inpatients with borderline personality disorder (BPD), but randomised trials have not been conducted.: Methods: Multicentre, double-blind, placebo-controlled trial. We aimed to ... ...

Abstract Background: Data from case series suggest that clozapine may benefit inpatients with borderline personality disorder (BPD), but randomised trials have not been conducted.
Methods: Multicentre, double-blind, placebo-controlled trial. We aimed to recruit 222 inpatients with severe BPD aged 18 or over, who had failed to respond to other antipsychotic medications. We randomly allocated participants on a 1:1 ratio to receive up to 400 mg of clozapine per day or an inert placebo using a remote web-based randomisation service. The primary outcome was total score on the Zanarini Rating scale for Borderline Personality Disorder (ZAN-BPD) at 6 months. Secondary outcomes included self-harm, aggression, resource use and costs, side effects and adverse events. We used a modified intention to treat analysis (mITT) restricted to those who took one or more dose of trial medication, using a general linear model fitted at 6 months adjusted for baseline score, allocation group and site.
Results: The study closed early due to poor recruitment and the impact of the COVID-19 pandemic. Of 29 study participants, 24 (83%) were followed up at 6 months, of whom 21 (72%) were included in the mITT analysis. At 6 months, 11 (73%) participants assigned to clozapine and 6 (43%) of those assigned to placebo were still taking trial medication. Adjusted difference in mean total ZAN-BPD score at 6 months was -3.86 (95% Confidence Intervals = -10.04 to 2.32). There were 14 serious adverse events; 6 in the clozapine arm and 8 in the placebo arm of the trial. There was little difference in the cost of care between groups.
Interpretation: We recruited insufficient participants to test the primary hypothesis. The study findings highlight problems in conducting placebo-controlled trials of clozapine and in using clozapine for people with BPD, outside specialist inpatient mental health units.
Trial registration: ISRCTN18352058. https://doi.org/10.1186/ISRCTN18352058.
Language English
Publishing date 2022-04-29
Publishing country England
Document type Journal Article
ZDB-ID 2646542-5
ISSN 2045-1261 ; 2045-1253
ISSN (online) 2045-1261
ISSN 2045-1253
DOI 10.1177/20451253221090832
Database MEDical Literature Analysis and Retrieval System OnLINE

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