Comparison of Target Controlled Infusio… | Clinical Trial

Key information

Conditions

Laparoscopic Surgery Target Controlled Infusion

Age range

3 year–12 year

Sex eligibility

All sexes

Study type

Observational

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

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.

Other names: TCI

Inhalation anesthetic

Drug

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

Other names: Sevoflurane

Primary outcomes

Modified Aldrete Scoring System

Time frame: Aftet surgery 1 hour

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.

Secondary outcomes

Blood pressure (mmHg)

Time frame: After surger 1 hour

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.
Heart rate (beats/minute)

Time frame: After surgey 1 hour

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.

Study contacts

Contact information is provided by the study sponsor or research team.

Özlem OZ GERGIN, MD

CONTACT

[email protected]

09005332466396

Sponsors and collaborators

Lead sponsor

TC Erciyes University

Other

Registry information

Official study 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

Important dates

Study start: 2024
Primary completion: 2025
Study completion: 2025
First posted: Aug 26, 2024
Registry last updated: Aug 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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