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Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures

RecruitingPhase 3Ages 3 Years - 17 YearsAllState University of New York at Buffalo
NCT07120763 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
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
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What it tests

  • Ketamine + Lidocaine
  • Ketamine group
  • Fentanyl (Nasalfent, Fentanyl Citrate Nasal Spray)
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Where

1 site
Oshei Children's Hospital
Buffalo, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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