Clinical Trials Directory

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UnknownNCT06073015

Effect of Esketamine on Reducing Postoperative Anxiety and Depression in Adolescent Patients

Status
Unknown
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Henan Provincial People's Hospital · Academic / Other
Sex
All
Age
8 Years – 18 Years
Healthy volunteers
Accepted

Summary

This study intends to conduct a prospective, double-blind, randomized, controlled trial. Adolescents aged 8-17 years old are selected as subjects. Esketamine is used as intervention before surgery, vital signs data, serum IL-6, CRP and other inflammatory indicators are collected during surgery, and the incidence and degree of anxiety and depression are evaluated after surgery. To determine the effect of esketamine on reducing anxiety and depression in adolescents after surgery, and to provide an effective clinical basis for accelerating the rehabilitation of adolescents after surgery.

Conditions

Interventions

TypeNameDescription
DRUGEsketamineGroup S received a subanesthetic dose of esketamine 0.2mg/kg (2ml/50 mg) 5 minutes before the procedure began.

Timeline

Start date
2023-10-10
Primary completion
2024-12-10
Completion
2025-02-10
First posted
2023-10-10
Last updated
2023-10-10

Source: ClinicalTrials.gov record NCT06073015. Inclusion in this directory is not an endorsement.