Carpal Tunnel Syndrome Carpal Tunnel Syndrome Vitamin D Ergocalciferols Randomized Controlled Trial Placebos Pain Measurement Grip Strength
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. adults with clinically diagnosed CTS based on characteristic symptoms and physical examination findings. Electrodiagnostic studies were performed when clinically indicated to confirm the diagnosis
Exclusion criteria
Exclusion criteria: 1. medical conditions requiring vitamin D supplementation, such as osteoporosis 2. diabetes mellitus 3. rheumatoid arthritis 4. pregnancy or breastfeeding 5. current use of anticonvulsants, rifampicin, or thrombolytic agents 6. known hypersensitivity to vitamin D or corn starch 7. receipt of vitamin D supplementation within 12 weeks prior to enrollment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity Baseline, 4 weeks, and 12 weeks after randomization Visual Analog Scale (VAS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Grip strength Baseline, 4 weeks, and 12 weeks after randomization JAMAR hydraulic hand dynamometer,Symptom severity Baseline, 4 weeks, and 12 weeks after randomization Thai version of the Boston Carpal Tunnel Questionnaire - Symptom Severity Scale (SSS),Functional status Baseline, 4 weeks, and 12 weeks after randomization Thai version of the Boston Carpal Tunnel Questionnaire - Functional Status Scale (FSS),Vitamin D toxicity At each follow-up visit during the 12-week treatment period Clinical monitoring of signs and symptoms of vitamin D toxicity | — |
Countries
Thailand
Contacts
Department of Orthopaedic Surgery, Panyananthaphikkhu Chonprathan Medical Center, Srinakharinwirot University