Local steroid injection in carpal tunnel syndrome with diabetes vs without diabetes
Official title: The Effect of Local Corticosteroid Injection on Electrophysiological and Ultrasonographic Findings in Carpal Tunnel Syndrome Patients With Type 2 Diabetes
Run by Haydarpasa Numune Training and Research Hospital · NCT07433257 · Data updated 2026-11-12
This study tests whether a corticosteroid and lidocaine injection helps people with carpal tunnel syndrome who also have type 2 diabetes as well as those without diabetes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Haydarpasa Numune Training and Research Hospital Academic / other |
| Locations | 1 site (Istanbul, Istanbul) |
| Status | Recruiting |
| Started | March 1, 2026 |
| Main results expected | July 31, 2026 |
| Study ends | July 31, 2026 |
| Registry record updated | May 27, 2026 |
| Trial ID | NCT07433257 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18-75 with mild-to-moderate CTS confirmed by electrophysiology, including those with type 2 diabetes (HbA1c < 7%), undergoing corticosteroid+lidocaine injection.
✕Probably not a fit
Patients with severe CTS, other neuropathies, cervical radiculopathy, or brachial plexopathy may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective observational study comparing recovery after a corticosteroid plus lidocaine injection between two groups: CTS patients with type 2 diabetes and CTS patients without diabetes. Participants have mild-to-moderate CTS confirmed by electrophysiology and receive a standard injection. Data are collected before treatment and at 4 and 12 weeks, including symptoms, function, and nerve measurements, to see if diabetes affects post-injection recovery. The study uses patient-reported outcomes and objective nerve studies to characterize differences in recovery trajectories between groups.
Why it matters
Potential benefit: If successful, the findings could help tailor expectations and management for CTS patients with diabetes.
How similar studies have gone: Other studies have explored injections for CTS, but this direct comparison between diabetic and non-diabetic CTS patients is less well established.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria * Carpal Tunnel Syndrome with Type 2 Diabetes Mellitus Group (Group 1): * Age between 18 and 75 years * Presence of clinical symptoms compatible with carpal tunnel syndrome (e.g., pain, paresthesia, numbness) for at least 3 months * Patients diagnosed with mild-to-moderate carpal tunnel syndrome based on electrophysiological findings * Diagnosis of type 2 diabetes mellitus * Regulated blood glucose levels, defined as hemoglobin A1c (HbA1c) \< 7% * Idiopathic Carpal Tunnel Syndrome Group (Group 2): * Age between 18 and 75 years * Presence of clinical symptoms consistent with carpal tunnel syndrome (e.g., pain, paresthesia, numbness) for at least 3 months * Patients diagnosed with mild-to-moderate carpal tunnel syndrome based on electrophysiological findings * No diagnosis of diabetes mellitus Exclusion Criteria * Severe carpal tunnel syndrome based on electrophysiological findings * Presence of polyneuropathy, cervical radiculopathy, brachial plexopathy, or thoracic outlet syndrome * Uncontrolled blood glucose levels in the diabetic group (hemoglobin A1c ≥ 7%) * Presence of another systemic disease, other than diabetes mellitus, that may cause carpal tunnel syndrome * Presence of a rheumatological disease * History of wrist surgery * Less than 6 months since a local corticosteroid injection for carpal tunnel syndrome * Less than 3 months since completion of a physical therapy program for carpal tunnel syndrome * Infection at the intended injection site * Presence of malignancy * Pregnancy
Where it's running
-
Istanbul Haydarpasa Numune Training and Research Hospital
Istanbul, Istanbul, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Talha Çeli̇k
- Email: talhacelikdr@gmail.com
- Phone: +905062398047
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.