Actively Recruiting
Comparison of the Efficacy of Ultrasound-Guided Corticosteroid Injection and Paraffin Therapy in Carpal Tunnel Syndrome
Led by Beylikduzu State Hospital · Updated on 2024-12-12
46
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating two treatments for carpal tunnel syndrome, a common nerve condition. This study compares the effectiveness and feasibility of paraffin therapy, a physical treatment, and ultrasound-guided corticosteroid injections, both considered low side-effect options. The trial involves adults aged 18 to 65 with mild to moderate symptoms confirmed by nerve studies. Participants will be grouped based on their treatment: either paraffin therapy or ultrasound-guided steroid injections. Assessments will be done at the start, 4 weeks, and 12 weeks after treatment to measure pain levels using the Visual Analog Scale (VAS) and functional ability with the Boston Carpal Tunnel Syndrome Questionnaire (BCTQ). Additional nerve function tests will be performed by a neurology specialist at 1 and 3 months without extra cost. During the study, participants will complete pain and function questionnaires and undergo electrophysiological evaluations measuring nerve response times and signal strengths. These tests help assess changes in nerve function over time. The study includes follow-ups outside working hours to reduce participant burden, and the total observation period lasts up to 12 weeks after treatment begins.
CONDITIONS
Brief Title
Comparison of the Efficacy of Ultrasound-Guided Corticosteroid Injection and Paraffin Therapy in Carpal Tunnel Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-65.
- Diagnosed with mild to moderate carpal tunnel syndrome based on electrophysiological studies.
- Received either ultrasound-guided corticosteroid injection or paraffin therapy.
- Symptoms persisting for at least 3 months.
You will not qualify if you...
- Diagnosis of other conditions causing neuropathic symptoms such as polyneuropathy, brachial plexopathy, or thoracic outlet syndrome.
- History of previous injection or surgery for carpal tunnel syndrome.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 weeks
Participants with carpal tunnel syndrome who received either ultrasound-guided corticosteroid injection or paraffin therapy are monitored to assess pain levels, functional impairment, and electrophysiological parameters.
Visits at baseline, 4th week, and 12th week
Trial Site Locations
Total: 1 location
1
Beylikdüzü State Hospital
Istanbul, Beylikdüzü, Turkey (Türkiye), 34147
Actively Recruiting
Research Team
B
Büşra Şirin Ahısha, MD
B
Büşra Şirin Ahısha
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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