Actively Recruiting
The Effect of Vibratory Anesthesia on Patient Pain Perception in Corticosteroid Injections of the Upper Extremity
Led by The University of Texas Medical Branch, Galveston · Updated on 2026-05-04
165
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research study focuses on adults with clinically diagnosed bilateral arthritis, tendinopathy, arthropathy, or compression neuropathy affecting the hand, wrist, or elbow. It aims to evaluate and compare the pain experienced at the injection site during corticosteroid injections using different anesthetic methods. The study investigates how different anesthesia modes may influence pain perception during these injections, which are part of standard medical care. Participants receive two corticosteroid injections, one in each arm, during a single visit. The study uses a randomized design to assign each injection to one of three anesthesia combinations: no anesthesia with vapocoolant spray, no anesthesia with vibration anesthesia using the DigiVibe device, or vapocoolant spray combined with vibration anesthesia. The DigiVibe device applies vibratory stimulation to the skin during the injection to potentially reduce pain. During the approximately 20-minute visit, participants complete numeric pain rating scales immediately after each injection to report their pain levels. Researchers measure pain intensity at injection sites on the hand, wrist, and elbow. Secondary measures assess changes in pain from before to after injection. The study collects data on pain perception to determine which anesthesia method is linked to the least discomfort during corticosteroid injections.
CONDITIONS
Brief Title
Vibratory Anesthesia on Pain Following Corticosteroid Injections
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Any patient with clinically diagnosed bilateral arthritis, tendinopathy, arthropathy, or compression neuropathy of the hand, wrist, or elbow where corticosteroid injection treatment is indicated
- Participants who voluntarily consent and sign consent forms
- Participants able to complete all numeric pain rating scales
- Patients aged 18 years or older
You will not qualify if you...
- Participants who opt out or withdraw consent
- Participants without capacity to consent to study participation or injection procedure
- Participants unable to complete numeric pain rating scales
- Participants allergic to triamcinolone acetonide, lidocaine, or bupivacaine
- Participants without clinically diagnosed bilateral arthritis, tendinopathy, arthropathy, or compression neuropathy of the hand, wrist, or elbow
- Participants where corticosteroid injection is not indicated bilaterally
- Patients younger than 18 years
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants receive two corticosteroid injections, one in each arm, during a single study visit. Different anesthesia methods are applied to each injection site based on random assignment. Participants complete pain rating scales immediately after each injection to assess pain and comfort.
1 visit (in-person, approximately 20 minutes)
Trial Site Locations
Total: 1 location
1
University of Texas Medical Branch
Galveston, Texas, United States, 77555
Actively Recruiting
Research Team
J
John Faillace, MD,FAAOS
A
Alice Lee
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
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