Actively Recruiting
Hematoma Block for Distal Radius Fracture
Led by Beth Israel Deaconess Medical Center · Updated on 2026-03-03
115
Participants Needed
1
Research Sites
695 weeks
Total Duration
On this page
Sponsors
B
Beth Israel Deaconess Medical Center
Lead Sponsor
H
Harvard University
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Hematoma Block for Distal Radius Fracture
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient 18 years old or older presenting to the emergency department with a distal radius fracture
You will not qualify if you...
- High acuity or distress as judged by the emergency physician
- Altered mental status or intoxication
- Aphasia, mental retardation, dementia, or inability to communicate
- Acute psychiatric illness
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215
Actively Recruiting
Research Team
B
Beatrice Hoffmann, MD
CONTACT
N
Nathan I Shapiro, MD MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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