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Esketamine: all studies

Page 20 of 123: studies 191 to 200 of 1,225, newest first. Back to the esketamine overview

Research

Intranasal esketamine for treatment-resistant depression: real-world effectiveness in electroconvulsive therapy non-responders

The European Journal of Psychiatry March 7, 2026 Rocío Gómez-juanes, Guillermo Mompaler Lázaro, Adoración Castro et al. 1 citation

Intranasal esketamine represents a novel therapeutic option for Treatment-Resistant Depression (TRD). However, its medium-to-long-term risk-benefit profile in real-world clinical practice remains controversial. Limited data is available regarding its effectiveness, particularly in patients who have not responded to electroconvulsive therapy (ECT), which is the focus of this study. We conducted...

Brain functional network correlates and predictors of the perioperative antidepressant effect of esketamine in breast cancer patients: a double-blind randomized controlled trial using resting-state fMRI and graph theory.

Translational Psychiatry March 6, 2026 Huimin Zhu, Qingfeng Wei, Shuang Xu et al. 1 citation

Postoperative depression adversely influences breast cancer patients' clinical outcomes. Our prior study demonstrated that intraoperative esketamine ameliorated postoperative depression in breast cancer patients, yet the underlying neural mechanism remains incompletely understood. We performed a double-blind randomized controlled trial in 35 breast cancer patients with preoperative depressive...

Effective doses of esketamine oral or esketamine intranasal for the prevention of preoperative anxiety in pediatric patients: A randomized double-blind dose-finding trial

Medicine March 6, 2026 Hongfei Xiong, Yingxue Xu, Jiayi Liu et al.

This study demonstrates the efficacy of single-dose esketamine regimens, administered orally (ED95: 8.2125 mg/kg; 95% CI: 7.4250-8.4597 mg/kg) and intranasally (ED95: 2.1770 mg/kg; 95% CI: 2.0952-2.1958 mg/kg), in mitigating preoperative anxiety within a pediatric population. These findings highlight the safety and efficacy of esketamine for this patient group.

Esketamine-based PCIA combined with intercostal nerve block for acute pain after lobectomy: a randomized controlled trial

Frontiers in Pharmacology March 4, 2026 Mi Zhou, Y M Qi, Fan Zhou et al.

Objective To evaluate outcomes of different doses of esketamine in postoperative patient-controlled intravenous analgesia (PCIA) combined with preoperative intercostal nerve block (ICNB) analgesia protocol for acute postoperative pain (APP) relief in patients undergoing thoracoscopic lobectomy. Materials and methods A total of 360 patients scheduled for thoracoscopic lobectomy at Xuzhou Central...

DOI: 10.3389/fphar.2026.1746121 (opens in new tab) Ketamine Randomized controlled trial Sufentanil Incidence geometry +11

Non-inferiority, comparative effectiveness study of intravenous ketamine v. intranasal esketamine for treatment-resistant depression: The EQUIVALENCE trial protocol.

Contemporary Clinical Trials March 2, 2026 Samuel T. Wilkinson, Sandhya Prashad, Rachel Dalthorp et al. 1 citation

Ketamine is a powerful and rapid-acting antidepressant but has no regulatory authorization for any psychiatric illness. The S-enantiomer of ketamine, esketamine, was approved by the FDA in 2019 as adjunctive therapy for treatment-resistant depression. Substantial controversy exists as to whether there is a significant clinical difference between intravenous (IV) ketamine racemate and intranasal...

DOI: 10.1016/j.cct.2026.108273 (opens in new tab) Ketamine Humans Antidepressive agents Administration, intranasal +6

Esketamine hydrochloride in the management of moderate-to-severe depressive symptoms in patients undergoing multiple wound repair surgeries: A multi-centre randomized, double-blind, placebo-controlled trial.

Clinical and translational medicine March 1, 2026 Xiaomeng Yu, Tianqi Shen, Ting Zhang et al.

Patients undergoing multiple wound repair surgeries often develop moderate-to-severe anxiety and depression. However, there is a lack of effective rapid emotional intervention strategies during the perioperative period. This multi-centre, randomized, double-blind, placebo-controlled trial involved 130 adult patients (65 in the esketamine group and 65 in the placebo group). Participants were...

DOI: 10.1002/ctm2.70641 (opens in new tab) Full text (opens in new tab) Esketamine Multiple trauma Postoperative complications Postoperative depression

Effects of Intraoperative Esketamine–Dexmedetomidine Combination on Postpartum Depressive Symptoms and Neuropsychiatric Events Following Cesarean Delivery: A Randomized Controlled Trial

Drug Design, Development and Therapy March 1, 2026 Meng-Meng Li, Qingfeng Wei, Qian-Yun Zhu et al.

Combined low-dose dexmedetomidine and esketamine during cesarean section provides a short-term improvement in early postpartum depressive symptoms, reduces intraoperative neuropsychiatric adverse events, and enhances maternal satisfaction, with a favorable maternal and neonatal safety profile.

DOI: 10.2147/dddt.s587487 (opens in new tab) Major depressive disorder Dexmedetomidine Adverse effect Randomized controlled trial +11

Ketamine and Esketamine Therapy in Affective Disorders: A Comprehensive Review of Mechanisms, Clinical Evidence, Safety, and Future Directions

Zenodo (CERN European Organization for Nuclear Research) February 28, 2026 Kshirsagar Pankaj*, Misal Shivdarshan, Dr. Giri Ashok preprint

Major Depressive Disorder (MDD) and Bipolar Depression represent significant global health burdens because about one-third of patients who receive standard monoaminergic antidepressant treatment fail to achieve remission. The population with Treatment-Resistant Depression (TRD) needs assistance because they deal with dangerous suicide risks and struggle with their daily activities. The review...

Adverse drug events and toxicological mechanisms of esketamine: a study based on US Food and Drug Administration Adverse Event Reporting System and network toxicology analysis.

Naunyn-Schmiedeberg's Archives of Pharmacology February 26, 2026 Lu Wang, Rui Xiong, Hengxu Liu et al. 1 citation

Esketamine is a novel antidepressant approved by the US Food and Drug Administration (FDA) in 2019, but comprehensive studies on the post-marketing safety evaluation of esketamine across age groups remain limited. The objective of this study is to provide the age-based pharmacovigilance profile of esketamine and the potential toxicological mechanisms, which may provide insights to inform the...

DOI: 10.1007/s00210-026-05108-z (opens in new tab) Esketamine Humans Antidepressive agents Age factors +7

Correction to: A real-world pharmacovigilance study of adverse events associated with esketamine: disproportionality analysis and detection of potential drug-drug interaction signals.

European Journal of Clinical Pharmacology February 23, 2026 Claudia Pisanu, Shungo Imai, Masami Tsuchiya et al. correction

Correction to: European Journal of Clinical Pharmacology (2026) 82:13 h t t p s : / / d o i . o r g / 1 0 . 1 0 0 7 / s 0 0 2 2 8 -0 2 5 -0 3 9 5 4 -z At page 13, the correct version of " 60 vs. 3 days, p < 0.001, Table 3" is "60 vs. 2 days, p < 0.001, Table 3).The original article can be found online at h t t p s : / / d o i . o r g / 1 0 . 1 0 0 7 / s 0 0 2 2 8 -0 2 5 -0 3 9 5 4 -z