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Effect of Different Administrations of Propofol on Emergence Agitation in Preschool Children Undergoing Ambulatory Surgery

NCT05420402 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2023-04-13

No results posted yet for this study

Summary

This study evaluates the influence of different dose and methods of propofol on emergence agitation(EA) through a randomized controlled trial when preschool children undergoing ambulatory surgery of inguinal hernia.

Conditions

  • Anesthesia
  • Surgery

Interventions

DRUG

Propofol bolus

A bolus dose of propofol 1 mg/kg was administered intravenously at 3 minutes before the end of the surgery.

DRUG

Propofol continuous infusion

1 mg/kg propofol was started by continuous infusion 3 minutes before the end of surgery, and the infusion time was 3 minutes.

DRUG

Propofol bolus

A bolus dose of propofol 1 mg/kg was administered intravenously at the end of the surgery.

Sponsors & Collaborators

  • Jiaxiang Chen

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
2 Years
Max Age
5 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-08-01
Primary Completion
2023-06-01
Completion
2023-06-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05420402 on ClinicalTrials.gov