Use of a Vibration Tool for Postoperative Pain Control in Distal Radius Fractures

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNorthwestern University

About this trial

The purpose of this research study is to determine if using a vibration tool improves pain control after surgical treatment of distal radius fracture. Additionally, the investigators would like to determine if this tool has any impact on consumption of pain medications postoperatively.

Eligibility criteria

Qualifiers

Patients with a distal radius fracture who have undergone an open reduction and internal fixation using a volar FCR approach with a single volar plate

Patients who can read, write, and follow direction in English

Willing to undergo occupational therapy at Northwestern Medicine's Hand Surgery clinic

Disqualifiers

Patients undergoing oncologic surgery

Patients who undergo simultaneous surgery such as open carpal tunnel

Patients who only require closed reduction of distal radius fractures

Operative patients that require dorsal plate fixation or separate radial styloid plate fixation

Trial design

Treatments tested in this trial

  • Vibration tool

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators