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Vibration Therapy for Postoperative Pain in Wrist Fractures

N/A
Waitlist Available
Led By Jason H Ko, MD, MBA
Research Sponsored by Northwestern University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
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
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 8 week post-surgery
Awards & highlights

Study Summary

This trial is testing whether using a vibration tool can help with pain control and reduce the need for pain medication after surgery for a broken radius bone.

Who is the study for?
This trial is for English-speaking patients who've had surgery to fix a broken wrist (distal radius fracture) using a specific technique with one plate. They must be willing to have occupational therapy at Northwestern Medicine's Hand Surgery clinic. It's not for those who had additional surgeries like carpal tunnel release or cancer-related procedures, or different types of wrist fixation.Check my eligibility
What is being tested?
The study is testing whether a vibration tool can help manage pain after wrist surgery. Researchers want to see if this tool reduces the need for pain medications during recovery.See study design
What are the potential side effects?
While the trial description does not specify side effects, generally, using a vibration tool may cause discomfort, temporary increase in pain, or skin irritation at the site of application.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I had surgery for a wrist fracture using a specific technique and plate.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 8 week post-surgery
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 8 week post-surgery for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
PROMIS Bank v1.1 - Pain Interference Computer Adaptive Test
PROMIS Bank v2.0 - Upper Extremity Computer Adaptive Test
Pain Visual Analog Scale (VAS)
+1 more
Secondary outcome measures
Opioid Use

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Vibration toolExperimental Treatment1 Intervention
Use of the vibration tool 3 times per day for 10 minutes for each session Morning, mid-day, and evening. Volarly for 5 minutes and dorsally for 5 minutes, for a total of 10 minutes during each session:
Group II: ControlActive Control1 Intervention
Standard of care, no vibration tool.

Find a Location

Who is running the clinical trial?

Northwestern UniversityLead Sponsor
1,585 Previous Clinical Trials
917,131 Total Patients Enrolled
Jason H Ko, MD, MBAPrincipal InvestigatorAssociate Professor

Media Library

Vibration tool Clinical Trial Eligibility Overview. Trial Name: NCT05318729 — N/A
Distal Radius Fracture Research Study Groups: Vibration tool, Control
Distal Radius Fracture Clinical Trial 2023: Vibration tool Highlights & Side Effects. Trial Name: NCT05318729 — N/A
Vibration tool 2023 Treatment Timeline for Medical Study. Trial Name: NCT05318729 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is this experiment presently seeking participants?

"Clinicaltrials.gov indicates that this research project is not accepting participants at the moment. This trial, which was initially posted on July 1st 2022 and last updated June 7th 2022, has yet to begin recruitment; however there are 859 other studies recruiting patients currently."

Answered by AI
~67 spots leftby Jul 2026