Comparison of the Efficacy of Peloid Therapy and Paraffin Treatment in Carpal Tunnel Syndrome
- Disease/Condition
- Carpal Tunnel Syndrome
- Drug/Device/Intervention
- physical therapy
- Study type
- Interventional
- Intervention type
- other
- Primary sponsor
- Beylikduzu State Hospital
- Location
- Istanbul, Turkey
- Phase
- N/A
- Start date
- Jun 01, 2024
- End date
- Oct 01, 2024
- Enrollment
- 60 participants
Boston Carpal Tunnel Syndrome Questionnaire
This study compares the effectiveness of peloid therapy and paraffin treatment in carpal
 tunnel syndrome. Patients receive either 2 weeks of peloid therapy or 15 sessions of paraffin
 treatment, along with splint therapy for 3 months. Pain and symptom severity are assessed
 using the Visual Analog Scale (VAS) and Boston Carpal Tunnel Syndrome Questionnaire (BCTQ).
 Results are measured at baseline, 4 weeks post-treatment, and a 12-week follow-up.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06405438
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06405438 through Pure Global AI's free database. This phase not specified trial is sponsored by Beylikduzu State Hospital and is currently Not yet recruiting. The study focuses on Carpal Tunnel Syndrome. Target enrollment is 60 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.