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Vibratory Anesthesia in Trigger Finger Injections

University of Arizona logo

University of Arizona

Status and phase

Enrolling
Phase 4

Conditions

Anesthesia, Local
Trigger Finger
Pain

Treatments

Device: Vibration Anesthesia Device by Blaine Labs
Drug: Gebauers Ethyl Chloride 100% Topical Spray

Study type

Interventional

Funder types

Other

Identifiers

NCT05405452
STUDY00001135

Details and patient eligibility

About

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.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,000 participants in 3 patient groups

No topical anesthesia
No Intervention group
Description:
No topical anesthesia will be given during the trigger finger injection.
Topical coolant
Experimental group
Description:
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.
Treatment:
Drug: Gebauers Ethyl Chloride 100% Topical Spray
Vibration
Experimental group
Description:
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.
Treatment:
Device: Vibration Anesthesia Device by Blaine Labs

Trial contacts and locations

2

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Central trial contact

Joey F Ghotmi, BS; Tolga Turker, MD

Data sourced from clinicaltrials.gov

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