Our study was planned as a prospective observational study aiming to compare the post-intervention recovery process between patients with carpal tunnel syndrome (CTS) and diabetes mellitus and patients with idiopathic carpal tunnel syndrome without diabetes mellitus. Patients who presented to the Physical Medicine and Rehabilitation outpatient clinic with clinical symptoms consistent with carpal tunnel syndrome and who were diagnosed with mild to moderate carpal tunnel syndrome based on electrophysiological findings and who received corticosteroid + local anesthetic injection will be included in the study. Data from patients who meet the inclusion and exclusion criteria will be included in the study. Patients' demographic and clinical data will be recorded. Records will be taken before treatment and at 4 and 12 weeks after treatment.
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Visual Analog Scale (VAS)
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment
Tinel Sign
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment
Phalen Test
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment
Boston Carpal Tunnel Syndrome Questionnaire (BCTSQ)
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment
Self-Administered Leeds Assessment of Neuropathic Symptoms and Signs (S-LANSS)
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment
Hand Grip Strength
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment
Pinch Strength
Timeframe: before treatment, 4 weeks after treatment, 12 weeks after treatment