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Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures

StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated October 10, 2025 (before its estimated August 22, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Primary completion date: Aug 30, 2026 to Aug 22, 2026
    • Study completion date: Aug 30, 2027 to Aug 22, 2027
    • Start date changed from estimate of Aug 30, 2025 to Aug 22, 2025
    • Site details revised
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07120763
Lead Sponsor State University of New York at Buffalo
Conditions
(from sponsor)		 Distal Radius Fracture Reduction, Pain Control, Pediatric Fractures
Related terms Agnosia
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov