NCT07268547
Wrist Reduction Intervention: Supracondylar Technique for Radial Nerve Block vs. Hematoma Block (WRIST Block Study)
Enrolling by Invitation
PHASE4Ages 18+InterventionalTreatmentSarasota Memorial Health Care SystemInvestigator-initiated
~105 participants
Updated 2025-12-15 on ClinicalTrials.gov
What's tested:Supracondylar radial nerve blockHematoma blockCombination of blocks
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Pain levels comparison
Measured over Pain will be measured at (1) baseline, (2) after administering the assigned pain block(s), and after the (3) fracture reduction.
Conditions
Where it's being run
1 sites across 1 statesFlorida1
Study leadership
- Aaron Grossberg, DO · PRINCIPAL_INVESTIGATOR · Sarasota Memorial Health Care System
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
18 years of age or older
Patients admitted to the ECC with a distal radius fracture requiring closed reduction
Patient must be willing and able to provide informed consent to the study
Exclusion
Under 18 years of age
Pregnant
Prisoner
Allergy to lidocaine
Patients unable to provide informed consent and/or perform study-related activities
Patients undergoing procedural sedation
Patients may be excluded at the discretion of the investigator based on their clinical judgment, if the participant no longer meets criteria, and/or if the health or safety of the patient may be impacted by taking part in the study.
What this trial measures
- Pain levels comparisonPain will be measured at (1) baseline, (2) after administering the assigned pain block(s), and after the (3) fracture reduction.
Comparing pain levels among patients who are undergoing a wrist fracture reduction. Measured on a scale of 0-10, 0= no pain to 10= worst pain. Pain will be measured at (1) baseline, (2) after administering the assigned pain block (s), and after the (3) fracture reduction.