Clinical Trial

"Supracondylar Radial Nerve Block Guided by Ultrasound Versus Hematoma Block for Analgesic Management in Closed Reduction of Distal Radius Fractures"

Recruiting
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Record status
This record was last updated March 17, 2025 (before its estimated March 31, 2025 completion). Its status may not reflect the trial's current state.
Summary
Non-surgical treatment with closed reduction and immobilization using a splint or cast is the preferred approach for stable distal radius fractures, particularly in elderly patients. It is also the initial intervention for displaced fractures with a surgical indication before the procedure, aiming to reduce edema, manage pain, and prevent associated complications. However, the maneuvers required for bone reduction can cause significant pain, and there is still insufficient evidence to favor one anesthetic method over another. In recent years, there has been a trend toward utilizing local methods, such as hematoma block or ultrasound-guided supracondylar block of the radial nerve, due to their lower incidence of complications. Nonetheless, there are currently no studies comparing the efficacy of these two analgesic approaches. This study aims to compare the analgesic effect of ultrasound-guided supracondylar block with that obtained through hematoma block in patients with distal radius fracture during closed reduction, using the Numeric Rating Scale. Additionally, it aims to compare the quality of the reduction through radiographic measures and assess the frequency of adverse events after the two interventions.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-02-26.
Trial Details
NCT Number NCT06857110
Lead Sponsor Hospital Universitario San Ignacio
Collaborators: Pontificia Universidad Javeriana
Conditions Distal Radius Fracture
Enrollment 50 participants
Start Date 2024-06-01
Primary Completion 2025-03-31 (estimated)
Study Completion 2025-06-30 (estimated)
Updated on ClinicalTrials.gov 2025-03-17