A phase 3 randomised double-blind placebo-controlled trial of mirtazapine as a pharmacotherapy for methamphetamine use disorder: A study protocol for the Tina Trial
Author:
McKetin Rebecca1ORCID, Degan Tayla2, Saunders Lucy2, Nguyen Long3, Dore Gregory2, Shoptaw Steven4, Farrell Michael5, Degenhardt Louisa2, Kelly Peter J6, Turner Alyna7, Clare Philip J8, Dean Olivia M7, Arunogiri Shalini9, Colledge-Frisby Samantha10, Koeijers Juanita5, Goodman-Meza David4, Sinclair Barbara11, Reid David11, Hill Harry12, Hayllar Jeremy13, Christmass Michael14, Cordaro Frank11, Lundin Robert7, Liaw Willy15, Liu Danica15, Holyoak Ellie13, Wu Brian Tid-Fung13, Kegan Joel5, Kontogiannis Ava6, Palmer Lily2, Morrison Caity7, Wrobel Anna7, Hyland Rebecca2, Byrne Marianne2, Zahra Emma1, Russell Samantha7, Berk Michael7
Affiliation:
1. University of New South Wales 2. University of New South Wales Medicine & Health 3. Burnet Institute 4. University of California Los Angeles 5. University of New South Wales Faculty of Medicine: University of New South Wales Medicine & Health 6. University of Wollongong Faculty of Health and Behavioural Sciences: University of Wollongong 7. Deakin University 8. The University of Sydney 9. Monash University 10. Curtin University School of Pharmacy and Biomedical Sciences: Curtin University Faculty of Health Sciences 11. NSW Health: New South Wales Ministry of Health 12. Barwon Health 13. Queensland Health 14. Western Australia Mental Health Commission 15. Drug and Alcohol Services South Australia
Abstract
Abstract
Background
There are no approved pharmacotherapies for methamphetamine use disorder. Two preliminary phase 2 randomised controlled trials have found mirtazapine, a tetracyclic antidepressant, to be effective in reducing methamphetamine use. The proposed Tina Trial is the first phase 3 placebo controlled randomised trial to examine the effectiveness and safety of mirtazapine as an outpatient pharmacotherapy for methamphetamine use disorder.
Methods
This is a multi-site phase 3 randomised, double-blind, placebo-controlled parallel trial. Participants are randomly allocated (1:1) to receive either mirtazapine (30 mg/day for 12 weeks) or matched placebo, delivered as a take-home medication. The target population is 340 people aged 18–65 years who have moderate to severe methamphetamine use disorder. The trial is being conducted through outpatient alcohol and other drug treatment clinics in Australia. The primary outcome is measured as self-reported days of methamphetamine use in the past 4 weeks at week 12. Secondary outcomes are methamphetamine negative oral fluid samples, depressive symptoms, sleep quality, HIV risk behaviour and quality of life. Other outcomes include safety (adverse events), tolerability, and health service use. Medication adherence is being monitored using MEMS® Smart Caps fitted to medication bottles.
Discussion
This trial will provide information on the safety and effectiveness of mirtazapine as a pharmacotherapy for methamphetamine use disorder when delivered as an outpatient medication in routine clinical practice. If found to be safe and effective, this trial will support an application for methamphetamine use disorder to be included as a therapeutic indication for the prescription of mirtazapine.
Trial Registration:
Australian and New Zealand Clinical Trials Registry (ACTRN12622000235707). Registered on February 9, 2022.
Publisher
Research Square Platform LLC
Reference37 articles.
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