CompletedNot Applicable

Laryngeal Mask Airway in Laparoscopic Hernia Repair

United States62 participantsStarted 2023-03-27

Plain-language 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.

Who can participate

Age range12 Months – 8 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Oxygen Saturation Measured by Pulse Oximetry in Percent Saturation

Timeframe: Patients will have oxygen saturation measured directly after placement airway device, the first oxygen saturation recorded five minutes after the start of surgery, and immediately prior to removal airway device, assessed up to 2 hours.

Trial details

NCT IDNCT06023394

SponsorChildren's Mercy Hospital Kansas City

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-05-08

Results submitted2025-03-05

View on ClinicalTrials.gov More Inguinal Hernia trials