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NCT06789185

Effects of Esketamine at Subanesthetic Dose on Emergence Delirium in Preschool Children Undergoing Ambulatory Laparoscopic Surgery

Completed NA Last updated 22 May 2025
What this trial tests

NA trial testing 0.1mg/kg esketamine in Inguinal Hernia in 96 participants. Completed in 16 May 2025.

Timeline
7 February 2025
Primary endpoint
16 May 2025
16 May 2025

Quick facts

Lead sponsorQiu jinpeng
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment96
Start date7 February 2025
Primary completion16 May 2025
Estimated completion16 May 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Qiu jinpeng — full company profile →

Who can join

Adults 24 Months to 71 Months, any sex, with Inguinal Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Emergence delirium (ED) is a manifestation of acute postoperative brain dysfunction that occurs with a relatively high frequency after pediatric anesthesia. The incidence varies depending on the diagnostic criteria used and the combination of administered anesthetic drugs. The goal of this clinical trial is to investigate whether a subanesthetic dose of esketamine can reduce incidence of ED.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Inguinal Hernia

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06789185.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing