Actively Recruiting
Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures
Led by State University of New York at Buffalo · Updated on 2025-10-10
50
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children requiring reduction for distal radius fracture
- Children presenting to the emergency department
- Children who are ages 3 to 17 years.
You will not qualify if you...
- Pediatric patients younger than 3 years old
- Adult patients aged 18 years or older
- Pediatric patients with injury patterns not suitable for hematoma block
- Children who cannot safely receive sedation due to BMI over the 95th percentile for age, ASA class greater than 2, Mallampati score greater than 2, or pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Oshei Children's Hospital
Buffalo, New York, United States, 14203
Actively Recruiting
Research Team
D
Dr. Ellen Lutnick Lutnick, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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