RecruitingPhase 3ketamine
Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures
Sponsored by State University of New York at Buffalo
NCT ID
NCT07120763
Target Enrollment
50 participants
Start Date
2025-08-22
Est. Completion
2027-08-22
About This Study
The aim of this study is to evaluate the efficacy of a hematoma block and minimal ketamine pain control or hematoma block and intranasal fentanyl in pediatric patients presenting with distal radius fractures requiring reduction, compared to control of standard full conscious sedation using ketamine.
Conditions Studied
Interventions
- •Ketamine + Lidocaine
- •Ketamine group
- •Fentanyl (Nasalfent, Fentanyl Citrate Nasal Spray)
Eligibility
Age:3 Years - 17 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * Children requiring reduction for distal radius fracture * Children presenting to the emergency department * Children who are ages 3 to 17 years. Exclusion Criteria: * Pediatric patients \<3 years old * Adult patients (i.e. ages 18 or up) * Pediatric patients with injury patterns that are not amenable to hematoma block. * Children who are not a candidate for sedation related to BMI \> 95%tile for age, ASA class \> 2, Mallampati score \> 2, and pregnant patients
Study Locations (1)
Oshei Children's Hospital
Buffalo, New York, United States