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Augmentation strategies for intravenous ketamine in treatment-resistant depression: A systematic review and meta-analysis.

Reinhard Janssen-Aguilar, Jithin Joseph, Huda Al-Shamali, Kaija Taylor, Zixu Zhao, Qiaowei Lin, Wendy Lou, Yanbo Zhang, Andrew J. Greenshaw, Walter Dunn, Robert Tanguay, Rakesh Jetly, Jennifer Swainson, Manish K. Jha, Venkat Bhat

Journal of Affective Disorders October 12, 2026 DOI: 10.1016/j.jad.2026.122619 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Systematic review and meta-analysis Randomized Peer reviewed
Sample size 346
Population Adults with treatment-resistant depression
Interventions Intravenous ketamine glutathione riluzole lamotrigine lithium D-cycloserine
Topics Depression Ketamine Esketamine
Keywords Augmentation strategies Randomized controlled trials
Key findings Across seven randomized trials, intravenous ketamine was associated with antidepressant improvement, but augmentation strategies generally did not add benefit over control conditions; an exploratory meta-analysis found no statistically significant overall difference in depressive symptoms (SMD -0.12; 95% CI -0.37 to 0.12). Ketamine combined with cognitive behavioral therapy or automated self-association training showed preliminary signals of improved maintenance of antidepressant effects, each evaluated in only one study. The authors conclude that low-certainty evidence is insufficient to support routine augmentation of intravenous ketamine for treatment-resistant depression.

Abstract

Treatment-resistant depression (TRD) affects 30-60% of individuals with major depressive disorder and carries substantial morbidity and healthcare costs. Intravenous (IV) ketamine (KET) is a rapid-acting antidepressant, but benefits are often transient, prompting augmentation to sustain efficacy or improve tolerability. We conducted a systematic review and meta-analysis of randomized controlled trials (RCTs) of IV KET augmentation in adults with TRD. MEDLINE, Embase, and PsycINFO were searched through October 29, 2025. Eligible studies compared KET plus augmentation with KET plus placebo/sham or active control. Seven RCTs (N = 346) met inclusion criteria. Strategies included glutathione, riluzole, lamotrigine, lithium, D-cycloserine and ketamine combined with psychotherapy (KCP) approaches involving cognitive behavioral therapy (CBT) and automated self-association training (ASAT). Across the included trials, IV KET was associated with antidepressant improvement, although augmentation strategies generally did not demonstrate additional benefit over their respective control conditions. Pharmacological augmentation strategies did not demonstrate additional benefit at primary endpoints. KCP approaches using CBT and ASAT yielded preliminary signals of improved maintenance of antidepressant effects, although each was evaluated in a single study. An exploratory random-effects meta-analysis of seven heterogeneous comparisons found no statistically significant overall difference in depressive symptoms between augmentation and control conditions (SMD = -0.12; 95% CI, -0.37 to 0.12; p = 0.323; I2 = 0.0%). No clear new safety signal emerged in the trials, although adverse-event reporting was heterogeneous across studies. Overall, low-certainty randomized evidence is insufficient to support routine augmentation of IV ketamine for TRD, highlighting the need for larger, rigorously designed trials to determine whether specific strategies can meaningfully extend ketamine's antidepressant effects.

In the evidence

This study is part of the evidence base for a synthesis in the library. Here is how each one recorded it.

  • Across seven RCTs, IV ketamine was associated with antidepressant improvement, but augmentation strategies generally added no benefit (overall SMD -0.12, 95% CI -0.37 to 0.12), with low-certainty evidence.

    Synthesized

Comparable studies

Other systematic reviews and meta-analyses on ketamine for depression, most cited first.

Study Year Design Participants
Ketamine and Other NMDA Antagonists: Early Clinical Trials and Possible Mechanisms in Depression Participants with major depression in placebo-controlled, double-blind, randomized... 2015 Systematic review and meta-analysis
Side-effects associated with ketamine use in depression: a systematic review. Patients with depression 2018 Systematic review
Comparative efficacy of racemic ketamine and esketamine for depression: a systematic review and meta-analysis Adults with unipolar or bipolar major depression 2020 Systematic review and meta-analysis n = 1,877
Single-dose infusion ketamine and non-ketamine N-methyl-D-aspartate receptor antagonists for unipolar and bipolar depression: a meta-analysis of efficacy, safety and time trajectories Patients with major depressive disorder or bipolar depression 2016 Systematic review and meta-analysis n = 588
The use of ketamine as an antidepressant: a systematic review and meta‐analysis People with major depressive disorder or bipolar disorder receiving ketamine infusion 2015 Meta-analysis n = 437

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