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Hematoma Block for Distal Radius Fracture

NCT02346929 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 115

Last updated 2026-03-03

No results posted yet for this study

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.

Conditions

  • Distal Radius Fracture

Interventions

OTHER

ultrasound guide

Patients randomized to this arm will have the hematoma block of the distal radial fracture with the guidance of a bedside ultrasound

Sponsors & Collaborators

Principal Investigators

  • Beatrice Hoffmann, MD · Beth Israel Deaconess Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2027-08-31
Completion
2027-12-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02346929 on ClinicalTrials.gov