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Not yet recruiting NCT06571682

Comparison of Target Controlled Infusion Anesthesia and Inhalation Anesthesia in Pediatric Laparoscopic Surgeries

Observational Laparoscopic Surgery Target Controlled Infusion

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Target Controlled Infusion, Inhalation anesthetic.
Who it may be relevant to
Registry conditions: Laparoscopic Surgery, Target Controlled Infusion. Basic parameters: 3 years — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of the Effect of Anesthesia Applied by Target Controlled Infusion Method and Inhalation Anesthesia Method on Patient Outcomes in Pediatric Patients Undergoing Laparoscopic Surgery

Overview

Comparison of Target Controlled Infusion Anesthesia and Inhalation Anesthesia in Pediatric Laparoscopic Surgeries

Detailed description

In pediatric age group patients undergoing laparoscopic surgery, total intravenous anesthesia (TIVA) and inhalation anesthesia methods are used as anesthesia methods in the intraoperative period; It is compared in terms of its effects on blood pressure, pulse, postoperative awakening time and awakening agitation.

Interventions

  • Device Target Controlled Infusion
    TCI (Target Controlled Infusion) is a method used to maintain the dose and rate of anesthesia drugs within a target concentration range set by the anesthetist. This system delivers drugs intravenously to the patient using a computer-controlled pump. The anesthetist adjusts the drug concentration to achieve the desired depth of anesthesia. This method provides more precise control over anesthesia and facilitates maintaining the depth of anesthesia within the desired range.
  • Drug Inhalation anesthetic
    In the inhalation anesthesia group, maintenance sevoflurane anesthesia will be applied after routine induction.

Primary outcome measures

  • Modified Aldrete Scoring System [Time frame: Aftet surgery 1 hour]
Secondary outcome measures (2)
  • Blood pressure (mmHg) [Time frame: After surger 1 hour]
  • Heart rate (beats/minute) [Time frame: After surgey 1 hour]

Eligibility criteria

Inclusion criteria

  • Children aged 3-12 years
  • Patients weighing over 10 kilograms
  • Patients who will undergo inguinal hernia surgery
  • ASA (American Society of Anesthesiologists) classification I and II pediatric patients.

Exclusion criteria

  • Absence of systemic illness.
  • ASA (American Society of Anesthesiologists) classification III and above pediatric patients.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06571682 · 2022/354

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗