Actively Recruiting
Effectiveness of Conservative Interventions in the Treatment of Trigger Finger
Led by Hacettepe University · Updated on 2025-09-09
54
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There is no study in the literature comparing the effectiveness of ESWT and splint therapy, which are the most commonly used approaches in the treatment of Trigger Finger (TF). The aim in this study is to investigate the effectiveness of ESWT and splint therapy used in the treatment of TF.
CONDITIONS
Official Title
Effectiveness of Conservative Interventions in the Treatment of Trigger Finger
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Volunteering to participate in the study
- Aged between 18 and 65 years
- Diagnosed with stage 1 or stage 2 Trigger Finger according to the Froimson classification
- Able to understand and respond to evaluation questionnaires
You will not qualify if you...
- Currently pregnant
- Having any inflammatory disorder
- Previous surgery on the hand or wrist
- Having a neurological disease
- Currently taking NSAIDs, painkillers, or similar medications
- Diagnosed with De Quervain's tenosynovitis or carpal tunnel syndrome
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Feray Karademir
Ankara, Ankara, Turkey (Türkiye), 06100
Actively Recruiting
Research Team
F
Feray Karademir
CONTACT
T
Tüzün Fırat
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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