Evidence map›Paper›PMID 41933313›Full record

ArticleBMC psychiatry2026

An international, double-blind, randomized, placebo-controlled clinical trial of adjunctive trimetazidine to treat people with bipolar depression (the TIDE trial) protocol.

Jee Hyun Kim, Chun Hui J Park, Preethi V Reddy, Sourav Khanra, Shyam Sundar Arumugham, Ganesan Venkatasubramanian, Monojit Debnath, Rashmi Arasappa, Melanie M Ashton, Bruna Panizzutti and 18 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMC psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Jee Hyun KimIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia. jee.kim@deakin.edu.au.
Chun Hui J ParkIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Preethi V ReddyDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Sourav KhanraDepartment of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, 834006, India.
Shyam Sundar ArumughamDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Ganesan VenkatasubramanianDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Monojit DebnathDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Rashmi ArasappaDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Melanie M AshtonIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Bruna PanizzuttiIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Alyna TurnerIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Varshitha TholasappaDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Devangi ShuklaDepartment of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, 834006, India.
Sachin Tudur SadashivaDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Justin RajDepartment of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, 834006, India.
Sudhakar DombaleDepartment of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, 834006, India.
Olivia DeanIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Mohammadreza MohebbiIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Eduard VietaBipolar and Depressives Disorders Unit, Hospital Clínic, University of Barcelona, Barcelona, Spain.
Isabella PacchiarottiBipolar and Depressives Disorders Unit, Hospital Clínic, University of Barcelona, Barcelona, Spain.
Shreekantiah UmeshDepartment of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, 834006, India.
Ken WalderIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia.
Lakshmi YathamDepartment of Psychiatry, University of British Columbia, Vancouver, BC, V6T 2A1, Canada.
Ji Hyun BaekDepartment of Psychiatry, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Gangnam-Gu, Seoul, 06351, Korea.
Nishant GoyalDepartment of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, 834006, India.
Y C Janardhan ReddyDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Muralidharan KesavanDepartment of Psychiatry, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, 560029, India.
Michael BerkIMPACT, The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC, 3220, Australia. michael.berk@deakin.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBipolar disorder is dominated by the depressive phase, and its treatment represents the greatest unmet need in mood disorders. Converging evidence indicates that bipolar depression is characterized by reduced mitochondrial function compared to the euthymic phase, with the severity of depressive symptoms correlated with the extent of mitochondrial dysfunction. Trimetazidine, a medication for angina pectoris, improves efficiency of mitochondrial energy generation and reduces oxidative stress and inflammation - addressing the three core biological features of bipolar depression. Thus, the Trimetazidine In bipolar DEpression (TIDE) trial repurposes trimetazidine to test its efficacy in treating bipolar depression.

methodsThe TIDE trial is a randomized, placebo-controlled, double-blinded, with a total recruitment target of 260 participants with bipolar disorder. Eligible participants will complete four visits and receive add-on trimetazidine or placebo across 8 weeks. Allocation to treatment arms will be randomized in a 1:1 ratio using permuted block randomization. An independent statistician will generate and retain the random allocation list. The trial biostatistician and clinicians, participants, their carers and physicians will be blinded to group allocations (i.e., a double-blind design). The effectiveness analysis will assess group differences (i.e., trimetazidine vs. placebo) in the primary outcome measure, the Montgomery Åsberg Depression Rating Scale total score, over the entire study period. The analysis will follow modified intention-to-treat principles and use a Generalized Estimating Equations (GEE) approach. Secondary outcomes include interviews and self-reports measuring global symptomology, anxiety symptoms, quality of life, day-to-day functioning, cognition, overall impairment, fatigue, cost effectiveness, and safety and tolerability data. DISCUSSION: Bipolar disorder is characterized by dysregulated energy metabolism, and trimetazidine is the first mitochondrial regulator identified as a potential drug to treat bipolar depression. Considering its established safety profile and novel target mechanism, a positive trial outcome may complement or even replace other options and offer an alternative for treating bipolar depression. If successful, its clinical impact could be global, improving health outcomes for hundreds of millions of people living with bipolar disorder.

trial registrationANZCTR ACTRN12622000474752, registered 25th March 2023.

Indexed as

Bipolar DisorderTrimetazidineAdultDouble-Blind MethodDrug Therapy, CombinationFemaleHumansMaleMiddle AgedMulticenter Studies as TopicRandomized Controlled Trials as TopicTrimetazidineBioenergeticsDepressionDrug repurposingEnergyInflammationMetabolismMitochondriaOxidative stressPsychiatryRandomized controlled trial

Identifiers

PMID41933313
PMCPMC13173853

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.