RecruitingPhase 4ACTRN12623001068651

Positioning of Esketamine Treatment (PoET) in the real-world management of depression

Evaluating the Positioning of Esketamine Treatment (PoET) for symptom management in adults with major depressive disorder


Sponsor

Northern Sydney Local Health District

Enrollment

162 participants

Start Date

Oct 31, 2023

Study Type

Interventional

Conditions

Summary

Depression is a common mental illness, and it is one of the leading causes of disease burden worldwide. Fortunately, there are many effective treatments available for depression, including lifestyle changes, psychological treatments, and medications such as antidepressants. However, not all patients will respond to the first treatment prescribed. Some patients may only experience a 'partial response', where a few treatments help their depression somewhat, but they do not achieve a full recovery. Currently, the reasons why some patients do not respond, or only experience a partial response to an antidepressant, is not fully understood. Recently, researchers have been investigating new medications that may help patients recover from depression. One of these new medications is Esketamine, which is a relatively new molecule derived from a drug called Ketamine - an anaesthetic that has been used medically for decades. Researchers have been investigating the antidepressant properties of Ketamine for a long time. It is thought that Ketamine, and its derivative, Esketamine, help to treat depression for a number of reasons. However, it is not yet known which patients benefit most from Esketamine when used in conjunction with conventional antidepressants. In addition, we do not yet understand how the effect of Esketamine is impacted by other treatments that a patient may be taking for their depression. Finally, it has not yet been investigated how patients with a partial response to an antidepressant will benefit from adding Esketamine to their therapeutic regimen without switching to a new baseline antidepressant. Therefore, there are two principle aims of this study 1) to investigate whether Esketamine is effective when added to ongoing antidepressant treatment and 2) to identify patient characteristics that will determine a therapeutic response to Esketamine in real-world practice. In patients that improve with the addition of Esketamine to their current antidepressant treatment, we hypothesize that their improvement will be determined by their personal characteristics and/or the type of treatment they are already receiving.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 65 Yearss

Plain Language Summary

Simplified for easier understanding

Esketamine is a newer antidepressant nasal spray that works through a completely different mechanism to traditional antidepressants — it acts quickly and has been approved for people whose depression has not responded to other treatments. While the drug has shown promise in clinical trials, questions remain about who benefits most from it when added on top of an existing antidepressant regimen, without having to switch medications first. The PoET study is a real-world observational study following adults aged 18–65 with major depressive disorder who are starting esketamine treatment. Researchers will track which patient characteristics and treatment histories are associated with the best outcomes, providing practical guidance for prescribing this treatment more effectively in everyday clinical practice. You may be eligible if you are 18–65 years old, have a primary diagnosis of major depression, are currently on antidepressant medication, have had an inadequate response to at least two previous antidepressants, and have not previously had psychosis, bipolar disorder, or substance misuse disorder. The study is run by Northern Sydney Local Health District.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

This is an uncontrolled, single arm, naturalistic study. There will be three treatment phases: Phase 1 - Acute treatment phase (weeks 1-4); Phase 2 - Maintenance treatment phase (weeks 5-8); Phase 3 -

This is an uncontrolled, single arm, naturalistic study. There will be three treatment phases: Phase 1 - Acute treatment phase (weeks 1-4); Phase 2 - Maintenance treatment phase (weeks 5-8); Phase 3 - Continuation treatment phase (Weeks 9-25). Phase 1 is the critical component of our study as it determines our primary outcomes. Name of drug: esketamine Dose: initial first dose is 56mg; subsequent doses will be 56mg or 84mg Duration: twice weekly for weeks 1-4; once weekly for weeks (5-8); once weekly/once fortnightly/once monthly as clinically indicated for weeks (9-25). After each treatment phase, participants will be re-assessed through a comprehensive battery of assessments and dose adjustments will be performed by the study psychiatrist based on tolerability, treatment response, and ongoing consent. Mode of administration: intranasal spray; self-administration with direct supervision Adherence to intervention: The intervention is dispensed and provided within the CADE clinic; therefore, participants' attendance at the clinic is required


Locations(1)

Royal North Shore Hospital - St Leonards

NSW, Australia

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ACTRN12623001068651


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