Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07553273

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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