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.
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