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Differences in Flare Reaction Incidence and Intensity Following Trigger Finger Injections - Trial NCT04900220

Access comprehensive clinical trial information for NCT04900220 through Pure Global AI's free database. This Phase 4 trial is sponsored by West Virginia University and is currently Recruiting. The study focuses on Trigger Finger. Target enrollment is 100 participants.

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NCT04900220
Phase 4
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT04900220
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Differences in Flare Reaction Incidence and Intensity Following Trigger Finger Injections
Investigating Differences in Flare Reaction Incidence and Intensity Following Trigger Finger Injections Using Betamethasone and Methylprednisolone

Study Focus

Trigger Finger

Betamethasone

Interventional

drug

Sponsor & Location

West Virginia University

Morgantown,Morgantown, United States of America

Timeline & Enrollment

Phase 4

Sep 15, 2021

Dec 01, 2022

100 participants

Primary Outcome

Incidence of pain,Intensity of pain,Peak of flare reaction,Resolution of flare reaction

Summary

Two common corticosteroids used for trigger finger treatment are betamethasone and
 methylprednisolone. Both injections are effective in treating trigger finger and the decision
 of which to use in treatment is currently a matter of the current practice and physician
 preference. The goal through this randomized trial is to see whether there is a difference
 between these two corticosteroids in inducing flare reactions and if there are any
 differences in the peak level of pain and their duration. Findings indicating a statistically
 significant difference in the incidence and/or intensity of the flare reactions would be
 clinically significant and would be evidence supporting the switch of current practice to one
 corticosteroid over the other.

ICD-10 Classifications

Trigger finger
Accessory finger(s)
Fused fingers
Accessory thumb(s)
Clubbing of fingers

Data Source

ClinicalTrials.gov

NCT04900220

Non-Device Trial