Comparing Inhalation and Total Intravenous Anesthesia Methods

Children Clinical Trial

Official title:

Comparison of Patient Outcomes Between Anesthesia Administered Via Target-Controlled Infusion Method and Inhalation Anesthesia Method in Pediatric Patients Undergoing Inguinal Hernia Repair.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06467279
• Other study ID #: 2022/200
• Status: Not yet recruiting
• Start date: July 15, 2024
• Est. completion date: February 15, 2025

Study information

• Verified date: June 2024
• Source: TC Erciyes University
• Contact: Özlem OZ Gergin, MD
• Phone: 09005332466396
• Email: oozgergin[@]erciyes.edu.tr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

comparison of Anesthesia by Target-Controlled Infusion and Inhalation Methods on Pediatric Patients Undergoing Inguinal Hernia Repair: Effects on Patient Outcomes

Description:

COMPARİSON OF THE EFFECT OF ANESTHESİA APPLİED BY TARGET CONTROLLED INFUSİON METHOD AND INHALATİON ANESTHESİA METHOD ON PATİENT OUTCOMES İN PEDİATRİC PATİENTS UNDERGOİNG INGUİNAL HERNİA REPAİR

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 60
• Est. completion date: February 15, 2025
• Est. primary completion date: December 15, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 3 Years to 12 Years

Eligibility

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 pediatric patients.

Related Conditions & MeSH terms

• Children
• Hernia
• Hernia, Inguinal

Intervention

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.

Locations

Country	Name	City	State
Turkey	Özlem OZ GERGIN	Kayseri?

Sponsors (1)

Lead Sponsor	Collaborator
TC Erciyes University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	after surgery 1 hours
Secondary	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.	after surgery 1 hours
Secondary	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.	after surgery 1 hours