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The Best Dose of Esketamine for Day Surgery of Pediatric Circumcision Pediatric Circumcision

Not Applicable
Completed
Conditions
Phimosis
Interventions
Registration Number
NCT04698434
Lead Sponsor
Yangzhou University
Brief Summary

In recent years, daytime operation has been developed gradually in China. Circumcision in children is a common type of daytime operation. The nature of the operation and the object of the operation determine that the anesthetic drugs used should induce fast, wake up quickly and recover in a high quality.

Esketamine is an S-enantiomer of ketamine, which is newly marketed in China. Compared with ketamine, it has stronger effect on NMDA receptor, and its sedative effect is about twice as high. The occurrence frequency of respiratory depression and hypotension is lower than that of other anesthetics and analgesics, which can provide good analgesic and sedative effect for surgical anesthesia.

In clinical practice, ketamine combined with sevoflurane has been widely used in children's microsurgery, but there has been no report on Esketamine combined with sevoflurane anesthesia.

In order to find out the best combined dose, this paper compares the single administration of three different doses of esketamine combined with sevoflurane anesthesia in the circumcision of children.

Detailed Description

To investigate the optimal dose of esketamine combined with sevoflurane for pediatric circumcision. Methods children who underwent day surgery of pediatric circumcision were randomly divided into 3 groups according to the random number table method:0.5mg/kg esketamine group (Group A), 0.75mg/kg esketamine group (Group B) and 1.0mg/kg of esketamine group (Group C), with 30 people in each group. mask inhalation of sevoflurane anesthesia, each group was given a single intravenous dose of the corresponding esketamine. Heart rate (HR), mean arterial pressure (MAP), pulse oxygen saturation (SpO2) and respiratory rate (RR) were recorded at room entry (T0), intravenous ketamine administration (T1), operation initiation (T2), intraoperative central ligation (T3) and operation completion (T4).The number and total amount of ketamine added intraoperatively were recorded. Duration of operation, time to open eyes and time to answer were recorded. The Eastern Ontario Children's Hospital pain Score (CHEOPS score) and the modified Bieri pain score were recorded when awake, 2 hours and 6 hours postoperatie. MOAA/S score was recorded at 15, 30 and 60min after surgery. Intraoperative and post-operative adverse reactions were recorded, including hypersensitivity, agitation, nausea and vomiting, dizziness, diplopia, etc.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
90
Inclusion Criteria
  • phimosis
Exclusion Criteria
  • cardiopathy
  • asthma
  • dysgnosia
  • surdimutism
  • hepatopathy or nephropathy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
0.5mg/kg esketamine groupEsketamine0.5mg/kg esketamine group will be given a single intravenous 0.5mg/kg esketamine
.75mg/kg esketamine groupEsketamine0.75mg/kg esketamine groupwill be given a single intravenous 0.75mg/kg esketamine
1.0mg/kg esketamine groupEsketamine1.0mg/kg esketamine group will be given a single intravenous 1.5mg/kg esketamine
Primary Outcome Measures
NameTimeMethod
recovery timeup to 2 hour

the time from stopping sevoflurane to resuscitation

Secondary Outcome Measures
NameTimeMethod
CHEOPS scoreup to 6 hours

The Eastern Ontario Children's Hospital Pain Score (CHEOPS score) at the time of 2h and 6h after surgery

Trial Locations

Locations (1)

Affiliated hospital of yangzhou university

🇨🇳

Yangzhou, Jiangsu, China

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