NCT07458152 Comparison of Wrist Splint Positions in Carpal Tunnel Syndrome
| NCT ID | NCT07458152 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Istanbul University |
| Condition | Carpal Tunnel Syndrome (CTS) |
| Study Type | INTERVENTIONAL |
| Enrollment | 108 participants |
| Start Date | 2026-03-01 |
| Primary Completion | 2029-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 108 participants in total. It began in 2026-03-01 with a primary completion date of 2029-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Carpal tunnel syndrome (CTS) is the most common nerve compression syndrome. It develops as a result of the compression of the median nerve while passing through the osteofibrous structure of the carpal tunnel located at the wrist. Sensory symptoms are the most prominent feature of CTS. These symptoms are observed as pain, paresthesia, and decreased sensory sensitivity. As motor symptoms, thumb abduction and opposition are primarily affected. In advanced cases, atrophy develops in the thenar muscles. Patients may describe weakness as difficulty in writing, opening jars, buttoning, or grasping objects. The diagnosis is made by fulfilling both clinical and electrophysiological diagnostic criteria. CTS has both conservative and surgical treatment options. Conservative treatment includes splinting, physical therapy modalities, and injection options, and it is preferred in mild and moderate cases. Among non-surgical treatment options, splint use is a commonly applied intervention; however, there is no consensus regarding its effectiveness, the optimal wrist position during use, or the duration and frequency of splint application. A total of 108 hands from patients aged 18 to 55 years diagnosed with CTS will be included in this study and randomized into three groups. All groups will be given an education and exercise program. The first group will use a wrist splint fixed at 15° flexion; the second group at neutral position; and the third group at 20° extension, to be worn only at night for eight weeks. Patients will be evaluated before treatment, immediately after treatment, and two months after the end of treatment using measures of pain- numbness severity, functional status, motor and sensory examination findings, and nerve conduction studies. What makes this study unique is that it evaluates the effects of splints that stabilize the wrist at different angles together with electrophysiological findings. A review of the literature shows that while some studies have examined and compared the effects of splints fixed at different wrist angles on symptoms, functional status, and physical examination findings, there is no study that evaluates these effects along with electrophysiological findings. Therefore, this study, which will compare the effectiveness of splints at different angles, is expected to contribute to the literature. The expected outcomes of this research are that one or more types of splints used in the conservative treatment of CTS will provide improvements in symptom severity, functional status, sensory and motor physical examination findings, and electrophysiological evaluation findings at the end of treatment.
Eligibility Criteria
Inclusion Criteria: * Diagnosis of mild to moderate carpal tunnel syndrome confirmed by electrophysiological studies performed within the last year. * Clinical findings consistent with carpal tunnel syndrome. * Age between 18 and 65 years. Exclusion Criteria: * \<18 years or \>65 years * Thenar atrophy * Surgery history for CTS * Steroid injection for CTS * Physical treatment for CTS in the last 6 months * Cervical radiculopathy * Tenosynovitis * Peripheral polyneuropathy * Another compressive neuropathy in the ipsilateral upper extremity * History of trauma/fracture to the hand-wrist region * Pregnancy * Metabolic disease * Rheumatic/autoimmune disease * Kidney failure
Frequently Asked Questions
Who can join the NCT07458152 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Carpal Tunnel Syndrome (CTS). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07458152 currently recruiting?
Yes, NCT07458152 is actively recruiting participants. Visit ClinicalTrials.gov or contact Istanbul University to inquire about joining.
Where is the NCT07458152 trial being conducted?
This trial is being conducted at Istanbul, Turkey (Türkiye).
Who is sponsoring the NCT07458152 clinical trial?
NCT07458152 is sponsored by Istanbul University. The trial plans to enroll 108 participants.