Clinical Trial

Impact of Esketamine on Delayed Neurocognitive Recovery in Older Patients

Not Yet Recruiting Phase 4
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Summary
Esketamine is frequently used during the perioperative period for supplemental analgesia. Small sample size trials showed that subanesthetic dose esketamine may decrease postoperative neurocognitive complications. However, conflicting results exist and optimal dose of esketamine remains to be determined. This dose-exploring pilot trial is designed to evaluate the safety and efficacy of three different perioperative esketamine dosing regimens in older patients undergoing major non-cardiac surgery. The primary purpose is to explore the optimal dosing strategy that produce maximal neurocognitive benefits with minimal adverse neuropsychiatric symptoms.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-04.
Trial Details
NCT Number NCT07523334
Lead Sponsor Peking University First Hospital
Collaborators: Tianjin Medical University General Hospital
Conditions Elderly, Noncardiac Surgery, Delayed Neurocognitive Recovery, Postoperative Delirium, Esketamine
Enrollment 120 participants
Start Date 2026-04
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-04-14