Differences in Flare Reaction Incidence and Intensity Following Trigger Finger Injections
- Disease/Condition
- Trigger Finger
- Drug/Device/Intervention
- Betamethasone
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- West Virginia University
- Location
- Morgantown,Morgantown, United States of America
- Phase
- Phase 4
- Start date
- Sep 15, 2021
- End date
- Dec 01, 2022
- Enrollment
- 100 participants
Incidence of pain,Intensity of pain,Peak of flare reaction,Resolution of flare reaction
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT04900220
- Type
- Non-Device Trial
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.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.