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Bayesian adaptive randomization trial of intravenous ketamine for veterans with late-life, treatment-resistant depression.

Brittany O'Brien, Charles E. Green, Rayan K. Al Jurdi, Lee C. Chang, Marijn Lijffijt, Sidra Iqbal, Tabish Iqbal, Alan C. Swann, Sanjay J. Mathew

Contemporary clinical trials communications December 1, 2019 DOI: 10.1016/j.conctc.2019.100432 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Adaptive randomization trial Peer reviewed
Population Older depressed veterans with late-life treatment-resistant depression
Interventions Ketamine Midazolam
Topics Depression Ketamine Esketamine
Keywords Adaptive design Bayesian trial design Late-life depression Veterans
Citations 10
Key findings The study is ongoing; results are expected to inform the viability of ketamine treatment and optimal dosing strategies for patients with late-life treatment-resistant depression.

Abstract

More than eleven million U.S. Veterans are at least 65 years of age, an age group of which almost 20% suffers from clinically significant depressive symptoms. Available pharmacological treatments are suboptimal for patients, including veterans, with late-life depression. Ketamine has emerged as a potentially promising rapid-acting therapy for treatment-resistant depression (TRD). However, few studies have examined the safety, tolerability and efficacy of ketamine therapy for older adults with late-life TRD (LL-TRD). This study uses an adaptive randomization design to test the safety, tolerability, efficacy, and durability of three distinct, single sub-anesthetic doses of intravenous (IV) ketamine versus a single dose of active placebo (midazolam) in older depressed veterans. As the study progresses, Bayesian adaptive randomization recalibrates randomization ratios to allocate more participants to conditions demonstrating greater promise and fewer participants to conditions with less promise. Secondary analyses explore clinical and biological moderating and mediating factors of rapid treatment response. Results are expected to inform both the viability of ketamine treatment and optimal dosing strategies for patients with LL-TRD.

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