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

Sponsor
Henan Provincial People's Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06073015
Collaborator
(none)
200
2
16.1

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effect of Esketamine on Reducing Postoperative Anxiety and Depression in Adolescent Patients
Anticipated Study Start Date :
Oct 10, 2023
Anticipated Primary Completion Date :
Dec 10, 2024
Anticipated Study Completion Date :
Feb 10, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

Esketamine (0.25mg/kg)

Drug: Esketamine
Group S received a subanesthetic dose of esketamine 0.2mg/kg (2ml/50 mg) 5 minutes before the procedure began.

No Intervention: Control group

the same volume of normal saline

Outcome Measures

Primary Outcome Measures

  1. Anxiety and depression scale scores 1 month after surgery [1 month]

    Anxiety and depression scale scores 1 month after surgery

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. 8 years ≤ age ≤17 years;

  2. Patients who plan to undergo elective surgery under general anesthesia, and the operation time is ≥2h;

  3. ASA grade I-II

Exclusion Criteria:
  1. Patients expected to be admitted to ICU after surgery;

  2. Patients who need to return to the ward with tracheal intubation after surgery;

  3. Allergic to the active ingredients or excipients of isketamine hydrochloride injection;

  4. Patients with severe consciousness disorder or mental system disease (schizophrenia, mania, bipolar disorder, psychosis, etc.) or cognitive dysfunction;

  5. Patients with congenital heart disease and severe developmental delay;

  6. Patients with one of the following contraindications to esketamine :(a) patients at risk of a significant increase in blood pressure or intracranial pressure; (b) Patients with ocular hypertension (glaucoma) or penetrating ocular trauma; (c) Patients with poorly controlled or untreated hypertension (resting systolic blood pressure greater than 180 mmHg or resting diastolic blood pressure greater than 100 mmHg); (d) Untreated or undertreated hyperthyroidism;

  7. Previous history of ketamine abuse or dependence, drug or alcohol dependence for more than 6 months, previous ketamine ineffective tests or adverse reactions.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Henan Provincial People's Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Henan Provincial People's Hospital
ClinicalTrials.gov Identifier:
NCT06073015
Other Study ID Numbers:
  • henanLYH
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 10, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 10, 2023