RECRUITING

Anesthetic Optimization in Pediatric LeFort Surgeries

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Anesthetic Optimization in Pediatric LeFort Surgeries

Quick Facts

Study Start:2025-05-02
Study Completion:2027-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05260320

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:14 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Undergoing Le Fort osteotomy at Johns Hopkins Hospital
  2. * Age \>= 14 years
  1. * Contraindications to standardized anesthetic protocol (intervention arm)

Contacts and Locations

Study Contact

Robin Yang, MD, DDS
CONTACT
443-997-9466
ryang14@jhmi.edu

Principal Investigator

Robin Yang, MD, DDS
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Johns Hopkins Hospital
Baltimore, Maryland, 21287
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Robin Yang, MD, DDS, PRINCIPAL_INVESTIGATOR, Johns Hopkins University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-02
Study Completion Date2027-07

Study Record Updates

Study Start Date2025-05-02
Study Completion Date2027-07

Terms related to this study

Additional Relevant MeSH Terms

  • Le Fort
  • Pain, Postoperative