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Laryngeal Mask Airway in Laparoscopic Hernia Repair

NCT06023394 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2025-04-03

Study results available
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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.

Conditions

  • Inguinal Hernia
  • Inguinal Hernia, Indirect
  • Inguinal Hernia Bilateral
  • Inguinal Hernia Unilateral

Interventions

DEVICE

Laryngeal Mask Airway

Laryngeal mask airway will be used as an airway device for Cohort A in the standard fashion.

DEVICE

Endotracheal Tube Device

Endotracheal tube airway will be used as an airway device for Cohort B in the standard fashion.

Sponsors & Collaborators

  • Children's Mercy Hospital Kansas City

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Months
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-27
Primary Completion
2024-05-08
Completion
2024-05-08
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06023394 on ClinicalTrials.gov