Comparing ultrasound guided and traditional hematoma blocks for pain relief in wrist fractures

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the effectiveness of ultrasound guided hematoma blocks compared to traditional 'blind' hematoma blocks for providing analgesia during the reduction of distal radius fractures. Hematoma blocks involve injecting lidocaine into the fracture line to alleviate pain, but can be challenging in cases of significant swelling. By utilizing ultrasound, the study seeks to enhance the precision and efficacy of this analgesic technique. The research will involve adult patients presenting with distal radius fractures in the emergency department.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult patient ≥ 18 years old presenting to the emergency department with complaint of distal radius fracture

Exclusion Criteria:

* High acuity/distress per the Attending ED physician
* Altered mental status or intoxication
* Aphasia, mental retardation, dementia, or insurmountable communication barrier
* Acute psychiatric illness

Where it's running

• Beth Israel Deaconess Medical Center
  Boston, Massachusetts, United States Recruiting

Study contacts

• Principal investigator: Beatrice Hoffmann, MD — Beth Israel Deaconess Medical Center
• Study coordinator: Beatrice Hoffmann, MD
• Email: bhoffma2@bidmc.harvard.edu
• Phone: 617-754-2323

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.