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Clinical Trials in Turkey / NCT07511764
Recruiting Not applicable

Comparison of Laryngeal Mask Airway Versus Endotracheal Intubation in Pediatric Laparoscopic Inguinal Hernia Repair

NCT07511764 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-01
Last updated
2026-06-24

Condition(s) studied

Inguinal Hernia Repair

Investigational drug(s) / intervention(s)

General Aneasthesia

General Aneasthesia: Laryngeal mask airway (LMA) or endotracheal intubation (ETT) in pediatric laparoscopic inguinal hernia repair

Study summary

Inguinal hernia is one of the most common conditions requiring surgical intervention in childhood, with a reported lifetime prevalence of 1-4%. With the increasing use of minimally invasive techniques such as PIRS (Percutaneous Internal Ring Suturing) among laparoscopic surgical procedures, perioperative anesthesia and airway management have become a critical area of clinical decision-making. The traditional approach in pediatric laparoscopic surgery is endotracheal intubation (ETT). Although ETT provides reliable airway control, it carries certain disadvantages. In contrast, the laryngeal mask airway (LMA) is less invasive and is associated with faster recovery. Systematic reviews and meta-analyses conducted in recent years have shown that the LMA may be safe for ventilation in pediatric laparoscopy, reduces peak airway pressure, and shortens recovery time. No well-designed, multicenter study with an adequate sample size comparing the LMA and ETT in pediatric laparoscopic inguinal hernia surgery has yet been conducted. This gap limits evidence-based decision-making in a clinical setting that directly impacts practice. Therefore, the aim of this study is to compare LMA and ETT in pediatric laparoscopic inguinal hernia repair. In this regard, the study is unique and necessary from both clinical and academic perspectives for determining the optimal airway strategy in pediatric laparoscopy.

Eligibility

Sex
ALL
Min age
1 Year
Max age
10 Years
Healthy volunteers
No
Inclusion Criteria: * being between 1 and 10 years of age, * having a planned laparoscopic inguinal hernia repair, * being classified as ASA I-II, * having given informed consent from the parent. Exclusion Criteria: * Obesity (body weight \>95th percentile), * symptomatic gastroesophageal reflux, * high risk of aspiration, * upper airway anomalies, * history of difficult intubation, * acute respiratory tract infection, * emergency surgical indication, * need for conversion from laparoscopy to open surgery, * presence of additional systemic risks such as immunodeficiency/malignancy.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dicle University Diyarbakır Eyalet/Yerleşke Recruiting

More Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07511764 on ClinicalTrials.gov ↗ ← All trials in Turkey