N/A
N=62
Laryngeal Mask Airway in Laparoscopic Hernia Repair
Inguinal Hernia · Inguinal Hernia, Indirect · Inguinal Hernia Bilateral · Inguinal Hernia Unilateral
Bottom Line
View on ClinicalTrials.gov: NCT06023394 ↗Enrolled (actual)
62
Serious AEs
0.0%
Results posted
Apr 2025
Primary outcome: Primary: Oxygen Saturation Measured by Pulse Oximetry in Percent Saturation — 100; 100; 100; 100 Percent Saturation
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Laryngeal Mask Airway (Device); Endotracheal Tube Device (Device)
- Age
- Pediatric · 0+ yrs
- Sex
- All
- Sponsor
- Children's Mercy Hospital Kansas City
- Primary completion
- May 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Oxygen Saturation Measured by Pulse Oximetry in Percent Saturation |
100; 100; 100; 100; 100; 100 | — |
| SECONDARY End-tidal Carbon Dioxide Measured by Capnography in mm Hg |
44; 43; 47; 48; 45; 49 | — |
| SECONDARY Peak Airway Pressure Will be Measured in cm H2O |
11; 14; 13; 16; 7; 11 | — |
| SECONDARY Documentation of Laryngospasm Occurrence |
0; 0 | — |
| SECONDARY Documentation of Oxygen Desaturation |
1; 1 | — |
Summary
This prospective randomized study will evaluate the effectiveness of laryngeal mask airway (LMA) versus endotracheal intubation (ETT) for patients undergoing laparoscopic inguinal hernia at CMH.
Eligibility Criteria
Inclusion Criteria
- Patients undergoing laparoscopic inguinal hernia repair.
- Ages 12 months to 8 years of age
- American Society of Anesthesiologists Physical Status Classification ASA 1 or 2
- ASA 1- A normal, healthy patient
- ASA 2- A patient with mild systemic disease
- Elective with appropriate NPO status
- English speakers
- Spanish speakers
Exclusion Criteria
- Patients with current gastroesophageal reflux
- Obesity (CDC >= 95th %ile)
- Contraindications to study protocol medications
Data sourced from ClinicalTrials.gov (NCT06023394). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.