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dc.contributor.authorQuested, Digby J
dc.contributor.authorSimpson, Jessica C
dc.contributor.authorCordey, Julia H
dc.contributor.authorEconomou, Alexis
dc.contributor.authorDe Crescenzo, Franco
dc.contributor.authorLawson, Jennifer
dc.contributor.authorAl-Taiar, Hasanen
dc.contributor.authorLennox, Alison
dc.contributor.authorGeddes, John R
dc.date.accessioned2020-07-15T14:59:56Z
dc.date.available2020-07-15T14:59:56Z
dc.date.issued2020-05
dc.identifier.citationDigby J. Quested, Jessica C. Gibson, Ann L. Sharpley, Julia H. Cordey, Alexis Economou, Franco De Crescenzo, Merryn Voyse , Jennifer Lawson, Jennifer M. Rendell , Hasanen Al‐Taiar , Alison Lennox, Farooq Ahmad, John R. Geddes. Melatonin In Acute Mania Investigation (MIAMI‐UK). A randomised controlled trial of add‐on melatonin in bipolar disorder. Bipoloar Disorders 31 May 2020en
dc.identifier.issn1399-5618
dc.identifier.urihttps://oxfordhealth-nhs.archive.knowledgearc.net/handle/123456789/515
dc.descriptionAvailable with an NHS OpenAthens log in for eligible usersen
dc.description.abstractObjectives Current options for treating emergent episodes of hypomania and mania in bipolar disorder are limited. Our objective was to compare the effectiveness and safety of add‐on melatonin in hypomania or mania over three weeks as a well‐tolerated therapy. Methods A randomised, double‐blind, parallel‐group, three‐week comparison of modified release melatonin (n=21) vs placebo (n=20) in adult bipolar patients aged 18‐65 years. Permuted block randomisation was used with participants and investigators masked to treatment allocation. Trial registration is ISRCTN28988273 and EUdraCT2008‐000281‐23. Approved by the South Central National Research Ethics Service (Oxford REC A) ref: 09/H0604/63. Results The trial was negative as there was no significant difference between melatonin and placebo on the primary outcome – mean Young Mania Rating Scale (YMRS) score at Day 21: (mean difference (MD) ‐1.77 ([95%CI:‐6.39 to 2.85]; p=0.447). Significantly fewer patients on melatonin scored 10 or more on the Altman Self Rating Mania Scale (ASRM): (odds ratio (OR) 0.164 [95% CI: 0.0260 to 1.0002]; p=0.05). Quick Inventory of Depression Symptomatology Clinician Version‐16 (QIDS‐C16) scores were not significantly different. (OR 1.77 [95% CI:0.43 to 7.29]; p=0.430). The proportion of patients scoring less than or equal to 5 on the self‐report QIDS‐SR16 at end‐point was greater for the melatonin group (OR 8.35[95% CI:1.04 to 67.23]; p=0.046). Conclusions In this small trial melatonin did not effectively treat emerging hypomania or mania as there was no significant difference on the primary outcome. The sample size limitation and secondary outcomes suggest further investigation of melatonin treatment in mood episodes is indicated.en
dc.description.sponsorshipSupported by the NIHRen
dc.description.urihttps://doi.org/10.1111/bdi.12944en
dc.language.isoenen
dc.subjectHypomaniaen
dc.subjectBipolar Disorderen
dc.titleMelatonin In Acute Mania Investigation (MIAMI‐UK). A randomised controlled trial of add‐on melatonin in bipolar disorderen
dc.typeArticleen


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