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Anesthetic Optimization in Pediatric LeFort Surgeries

Johns Hopkins University · NCT05260320

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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
Anesthetic Optimization in Pediatric LeFort Surgeries (NCT05260320) | Bored Studies