RecruitingNot ApplicableNCT02346929

Hematoma Block for Distal Radius Fracture

Comparison of Ultrasound-guided Hematoma Block and "Blind" Hematoma Block for Analgesia in Distal Radius Fractures

Sponsor

Beth Israel Deaconess Medical Center

Enrollment

115 participants

Start Date

Aug 1, 2014

Study Type

INTERVENTIONAL

Conditions

Distal Radius Fracture

Summary

The purpose of this study is to determine the efficacy of ultrasound guided hematoma block versus traditional "blind" hematoma block for analgesia in distal radius fracture reduction.

Eligibility

Min Age: 18 YearsMax Age: 100 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying ultrasound guide for people with distal radius fracture. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 100 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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