Anesthetic Optimization in Pediatric LeFort Surgeries
Johns Hopkins University · NCT05260320
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 14+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 50
- US sites recruiting
- 1
- Study start
- May 2, 2025
- Record last updated
- May 20, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Standardized Anesthetic Course from Premedication to Induction
Conditions: Le Fort; Pain, Postoperative
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Undergoing Le Fort osteotomy at Johns Hopkins Hospital
- Age >= 14 years
Exclusion Criteria
- Contraindications to standardized anesthetic protocol (intervention arm)
Recruiting US locations
Johns Hopkins Hospital
Baltimore, MD 21287
Site contact: Robin Yang, MD, DDS · 443-997-9466 · ryang14@jhmi.edu
Study contacts (from the official record)
- Robin Yang, MD, DDS · 443-997-9466 · ryang14@jhmi.edu
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