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

Author:

Crawford Mike J.1ORCID,Leeson Verity C.2,Evans Rachel3,Barrett Barbara4,McQuaid Aisling2,Cheshire Jack5,Sanatinia Rahil2,Lamph Gary6,Sen Piyal7,Anagnostakis Katina8,Millard Louise8,Qurashi Inti9,Larkin Fintan10,Husain Nusrat11,Moran Paul12,Barnes Thomas R.E.2ORCID,Paton Carol2,Hoare Zoe3,Picchioni Marco13,Gibbon Simon5

Affiliation:

1. Division of Psychiatry, Imperial College London, The Commonwealth Building, The Hammersmith Hospital, Du Cane Road, London W12 0NN, UK

2. Division of Psychiatry, Imperial College London, London, UK

3. North Wales Organisation for Randomised Trials in Health, Bangor University, Bangor, UK

4. King’s Health Economics, King’s College London, London, UK

5. Department of Forensic Psychiatry, Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, UK

6. School of Nursing, University of Central Lancashire, Preston, UK

7. Department of Forensic Psychiatry, Elysium Healthcare, Milton Keynes, UK

8. St Andrew’s Academic Centre, St Andrew’s Healthcare, Northampton, UK

9. Ashworth Hospital, Mersey Care NHS Foundation Trust, Liverpool, UK

10. Acute Mental Health Services, West London NHS Trust, London, UK

11. Division of Psychology & Mental Health, University of Manchester, Manchester, UK

12. Centre for Academic Mental Health, University of Bristol, Bristol, UK

13. Department of Forensic and Neurodevelopmental Science, Kings College London, London, UK

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

Funder

National Institute for Health Research

Publisher

SAGE Publications

Subject

Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Psychology (miscellaneous)

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