Comparative Evaluation of Finger Splint, Paraffin, and Peloidotherapy Interventions in the Management of Trigger Finger

Recruiting N/A Interventional Study
Trigger Finger Splint Therapy Paraffin Bath Peloidotherapy Efficacy and Safety Randomised Clinical Trial
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 75
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
60 (estimated)
Sponsor
Konya Beyhekim Training and Research Hospital · Government
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About This Trial
Patients aged 18-75 years who present with trigger finger to a tertiary rehabilitation hospital and agree to participate will be included in the study. Participants will be randomly allocated into three groups using block randomization. The first group will use a static finger splint that blocks the proximal interphalangeal joint for 6 weeks, along with a home exercise program. The second group wi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Being between 18 and 75 years of age and willing to participate in the study * Having a diagnosis of idiopathic single trigger finger, Grade 2-3 Exclusion Criteria: * Patients with triggering in more than one finger * Patients with triggering at the A3 pulley or with Grade 1…
Contacts

Ramazan Yilmaz, Assoc Prof (MD)

+905556232674

drramazanyilmaz@yahoo.com

CONTACT