Carpal tunnel syndrome. Carpal tunnel syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Agreement for participation in the study Age of 20 to 65 years old Diagnosing patients with carpal tunnel syndrome by a neurologist: Carpal tunnel syndrome severity: Mild, moderate, or severe.
Exclusion criteria
Exclusion criteria: Not attending follow-up appointments during various phases of the study Reaction and sensitivity to the prescribed supplement Non-compliance with recommendations and nutritional supplements Suffering from cardiovascular diseases, blood pressure, diabetes, liver, kidney, thyroid, malignancies and other neurological disorders smoking Cervical radiculopathy - Wrist fractures - Previous median nerve injury Presence of trigger points in muscles mimicking CTS symptoms
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of disease. Timepoint: At baseline and after 14 days. Method of measurement: Boston Carpal Tunnel Questionnaire.;Serum level of C-reactive protein (CRP). Timepoint: At baseline and after 14 days. Method of measurement: Enzyme-linked immunosorbent assay (ELISA) kits.;Total antioxidant capacity. Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Total oxidant status. Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Muscle nerve band. Timepoint: At baseline and after 14 days. Method of measurement: Electromyography.;Malondialdehyde. Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Serum concentration of glutathione. Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Superoxide dismutase activity. Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Serum level of vascular cell adhesion molecule-1. Timepoint: At baseline and after 14 days. Method of measurement: Enzyme-linked immunosorbent assay (ELISA) kits.;Erythrocyte sedimentation rate (ESR). Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Thyroid hormones. Timepoint: At baseline and after 14 days. Method of measurement: biochemical kit of KiaZist Co.;Serum level of IL-6. Timepoint: At baseline and after 14 days. Method of measurement: Enzyme-linked immunosorbent assay (ELISA) kits.;Serum level of TNF-a. Timepoint: At baseline and after 14 days. Method of measurement: Enzyme-linked immunosorbent assay (ELISA) kits.;Serum level of TGF. Timepoint: At baseline and after 14 days. Method of measurement: Enzyme-linked immunosorbent assay (ELISA) kits. | — |
Secondary
| Measure | Time frame |
|---|---|
| The average level of total cholesterol (HDL, LDL, TG) in the intervention and control groups. Timepoint: before and after intervention. Method of measurement: Kiazist biochemical kit.;The mean level of fasting blood sugar (FBS) among the intervention and control groups. Timepoint: Before and after intervention. Method of measurement: Kiazist biochemical kit. | — |
Countries
Iran (Islamic Republic of)
Contacts
Esfahan University of Medical Sciences