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Efficacy and tolerability of ketamine in moderate to severe obsessive-compulsive disorder: a systematic review.

Shayan Eghdami, Mahsa Boroon, Amir-Abbas Keshavarz-Akhlaghi, Mohammadreza Shalbafan

Psychopharmacology August 27, 2026 DOI: 10.1007/s00213-026-07155-z (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Systematic review Randomized Open-label Longitudinal Peer reviewed
Sample size 118
Population Patients with moderate to severe obsessive-compulsive disorder
Intervention Ketamine
Dose 0.5 mg/kg single-dose intravenous
Topics Ketamine Esketamine
Keywords Adverse effects Drug therapy Glutamates N-methyl-d-aspartate Obsessive-compulsive disorder Systematic-review as topic
Key findings Single-dose intravenous ketamine (0.5 mg/kg) yields rapid anti-obsessional response rates of 50-60%, but benefits from monotherapy are typically transient, dissipating within one week. Combining ketamine with exposure and response prevention (ERP) produced sustained remission lasting weeks to months, suggesting a synergistic effect. The authors identified a safety signal of delayed-onset dysphoria and suicidal ideation 24-48 hours post-infusion in a subset of patients.

Abstract

Approximately 40-60% of patients with obsessive-compulsive disorder (OCD) fail to respond to standard serotonergic and behavioral therapies. This systematic review evaluates the efficacy, durability, and safety of ketamine, a glutamate modulator, for moderate to severe OCD. Following PRISMA guidelines, we searched electronic databases through January 2026 for studies treating moderate-to-severe OCD with ketamine. Fifteen studies were included (three RCTs, four open-label trials, and eight case reports), comprising 118 participants. Randomized trials demonstrated that single-dose intravenous ketamine (0.5 mg/kg) yields rapid anti-obsessional response rates of 50-60%. However, benefits from monotherapy were typically transient, often dissipating within one week. Conversely, protocols integrating ketamine with concurrent exposure and response prevention (ERP) reported sustained remission lasting weeks to months, suggesting a synergistic effect. While intravenous and oral routes were effective, intranasal administration faced high refusal rates due to contamination fears. Safety analysis identified a specific signal of delayed-onset dysphoria and suicidal ideation (24-48 hours post-infusion) in a subset of patients, distinct from depression trials. Ketamine may provide positive but short-lived symptom relief for moderate to severe OCD when used as a standalone intervention. Its clinical utility may be greatest when used as a pharmacological adjunct to behavioral therapy, potentially creating a therapeutic window that may facilitate effective ERP. Clinicians should implement extended monitoring for delayed psychiatric adverse events. Further longitudinal and mechanistic studies are warranted to delineate ketamine's optimal dosing parameters, timing, and integration strategies within multimodal OCD treatment frameworks.

Comparable studies

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

Study Year Design Participants
The effect of a single dose of intravenous ketamine on suicidal ideation: a systematic review and individual participant data meta-analysis Depressed patients with suicidal ideation at baseline 2017 Systematic review and individual participant data meta-analysis n = 167
Ketamine use: a review Ketamine users 2011 Systematic review
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
Ketamine and postoperative pain – a quantitative systematic review of randomised trials Surgical patients from 25 countries 2004 Systematic review n = 2,839
Side-effects associated with ketamine use in depression: a systematic review. Patients with depression 2018 Systematic review

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