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

ConditionsLaparoscopic SurgeryTarget Controlled Infusion
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-12
SponsorTC Erciyes University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

Absence of systemic illness.

ASA (American Society of Anesthesiologists) classification III and above pediatric patients.

Trial population

Children aged 3-12 with ASA I-II undergoing laparoscopic surgery

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Target Controlled Infusion

    Device

    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.

  • Inhalation anesthetic

    Drug

    In the inhalation anesthesia group, maintenance sevoflurane anesthesia will be applied after routine induction.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Total Intravenous Anesthesia Group1 intervention
Group B: Inhalation Anesthesia Group1 intervention

Trial outcomes

Primary outcomes

1

Modified Aldrete Scoring System

The effects on recovery were monitored within the first hour of the postoperative period using the Modified Aldrete Scoring System (MASS). Totally 0-10 points can be given by MASS. Higher scores predicts better recovery.

Time frame
Aftet surgery 1 hour

Secondary outcomes

1

Blood pressure (mmHg)

The blood pressure of the patients will be measured and recorded in mmHg at five-minute intervals from the beginning until the first postoperative hour.

Time frame
After surger 1 hour
2

Heart rate (beats/minute)

The heart rate of the patients will be measured and recorded in mmHg at five-minute intervals from the beginning until the first postoperative hour.

Time frame
After surgey 1 hour

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

TC Erciyes University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: