Anesthetic Optimization in Pediatric LeFort Surgeries
Recruiting
N/A
Interventional Study
Le Fort
Pain, Postoperative
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 14 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 50 (estimated)
- Sponsor
- Johns Hopkins University · Other
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About This Trial
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, inpatie…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Undergoing Le Fort osteotomy at Johns Hopkins Hospital
* Age \>= 14 years
Exclusion Criteria:
* Contraindications to standardized anesthetic protocol (intervention arm)
Contacts