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
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
Inclusion Criteria1
- Adult patient ≥ 18 years old presenting to the emergency department with complaint of distal radius fracture
Exclusion Criteria4
- High acuity/distress per the Attending ED physician
- Altered mental status or intoxication
- Aphasia, mental retardation, dementia, or insurmountable communication barrier
- Acute psychiatric illness
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Interventions
OTHERultrasound guide
Patients randomized to this arm will have the hematoma block of the distal radial fracture with the guidance of a bedside ultrasound
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT02346929
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