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Clinical Trials/NCT05405452
NCT05405452
Recruiting
Phase 4

Investigation of the Effectiveness of Vibratory Stimulus in Trigger Finger Injections

University of Arizona2 sites in 1 country1,000 target enrollmentAugust 14, 2023

Overview

Phase
Phase 4
Intervention
Gebauers Ethyl Chloride 100% Topical Spray
Conditions
Trigger Finger
Sponsor
University of Arizona
Enrollment
1000
Locations
2
Primary Endpoint
Pain Felt
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This study aims to compare the effectiveness of the use of no topical anesthesia, topical coolant, and the use of vibration in the reduction of pain during trigger finger injections. This will be done by randomizing patients who are diagnosed with trigger finger, warrant and choose to continue with a steroid injection into each of the respective anesthetic (or lack thereof) methods described. After conducting this and gathering data on the subjects pain felt, we will compare the analgesia from each of the anesthetic methods.

Registry
clinicaltrials.gov
Start Date
August 14, 2023
End Date
August 1, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tolga Turker

Associate Professor

University of Arizona

Eligibility Criteria

Inclusion Criteria

  • Healthy Adult
  • Diagnosed with trigger finger
  • Warrants a trigger finger injection

Exclusion Criteria

  • Subjects with known decreased light touch sensation in the territory of the trigger finger injection.
  • Not diagnosed with trigger finger or does not warrant a trigger finger injection per the typical treatment algorithm adopted by the attending physician.

Arms & Interventions

Topical coolant

The subject will have 5 seconds of sterile ethyl chloride sprayed at the site of the trigger finger injections just prior to the administration of the injection.

Intervention: Gebauers Ethyl Chloride 100% Topical Spray

Vibration

The subject will have a vibration device placed just proximal to the site of the trigger finger injection concurrent with the administration of the injection.

Intervention: Vibration Anesthesia Device by Blaine Labs

Outcomes

Primary Outcomes

Pain Felt

Time Frame: Immediately after the trigger finger injection is completed

Visual Analog Pain Scale Rating (Hayes and Patterson 1921) Scale Title: Pain scale Maximum Value: 10 - The worst pain Minimum value: 0 - No pain \*A lower number indicates a better outcome (less pain felt).

Study Sites (2)

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