Overview

Opioid Reduction Initiative During Outpatient Pediatric Urologic Procedures Using Exparel

Status:
Recruiting
Trial end date:
2023-07-01
Target enrollment:
0
Participant gender:
All
Summary
This study aims to evaluate the utility of long-acting liposomal bupivacaine (Exparel®) in improving pain scores and reducing narcotic pain requirements in pediatric patients following minor urologic procedures.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Johns Hopkins University
Treatments:
Bupivacaine
Criteria
Inclusion Criteria:

- Pediatric patients 6 years and older undergoing minor pediatric urologic surgery

- Patients who are otherwise eligible to receive routine care following minor urologic
surgery

Exclusion Criteria:

- Contraindication to receiving local anesthetics (i.e. pre-existing cardiac, renal,
hepatic dysfunction)

- Pediatric patients younger than 6 years of age

- Pediatric patients with a history of pain syndromes or are unable to tolerate opiate
medication

- Unwilling to participate in 48 hours and 10-14 day follow-up phone calls