RecruitingNot ApplicableNCT05260320

Anesthetic Optimization in Pediatric LeFort Surgeries

Sponsor

Johns Hopkins University

Enrollment

50 participants

Start Date

May 2, 2025

Study Type

INTERVENTIONAL

Conditions

Pain, Postoperative Le Fort

Summary

This study will propose and evaluate a standardized LeFort osteotomy anesthetic protocol for pediatric patients at Johns Hopkins Hospital. There are two cohorts to this study: a prospective cohort who will receive the study anesthesia protocol and a historical cohort that received standard of care. The investigators hope this will help to minimize unnecessary postoperative pain management, inpatient stay, and long-term morbidity and mortality in these patients.

Eligibility

Min Age: 14 Years

Plain Language Summary

Simplified for easier understanding

This study examines the best anesthetic approach for young patients undergoing LeFort osteotomy at Johns Hopkins Hospital. LeFort surgery is a procedure that repositions the bones of the mid-face to correct structural problems affecting breathing, chewing, or appearance. The study aims to optimize how patients are put to sleep and managed during surgery to reduce complications and improve recovery. You may be eligible if: - You are 14 years of age or older - You are scheduled to undergo a LeFort osteotomy at Johns Hopkins Hospital You may NOT be eligible if: - You have a specific medical condition that prevents use of the standardized anesthetic protocol used in this study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.