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Enrolling By InvitationNCT07268547

Wrist Reduction Intervention: Supracondylar Technique for Radial Nerve Block vs. Hematoma Block (WRIST Block Study)

Status
Enrolling By Invitation
Phase
Phase 4
Study type
Interventional
Enrollment
105 (estimated)
Sponsor
Sarasota Memorial Health Care System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare different types of local anesthesia-a supracondylar radial nerve block, a hematoma block, or a combination of the two-for reducing pain in people with a broken wrist (distal radius fracture). This is being done to find out which method provides better pain relief after the injury and during treatment in the emergency room.

Detailed description

This study is testing different ways to provide pain relief before reducing a broken wrist. Participants will receive one of three techniques: (1) a nerve block where a doctor injects lidocaine near the radial nerve under ultrasound guidance; (2) a hematoma block where a doctor injects lidocaine into the area where the bone broke; or (3) both the nerve block and the hematoma block. Patients will be asked how much pain they feel before the numbing, after the numbing, and after the wrist is reduced.

Conditions

Interventions

TypeNameDescription
PROCEDURESupracondylar radial nerve blockSupracondylar radial nerve blocks given at the radial nerve not as the same location of the fracture site, prior to fracture reduction.
PROCEDUREHematoma blockInjection of analgesia into the hematoma that forms surrounding the wrist fracture.
PROCEDURECombination of blocksSupracondylar radial nerve block given first, followed by hematoma block, before fracture reduction.

Timeline

Start date
2025-12-09
Primary completion
2027-12-01
Completion
2027-12-01
First posted
2025-12-05
Last updated
2025-12-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07268547. Inclusion in this directory is not an endorsement.