Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:52 PM
Ignite Modification Date:
2025-12-24 @ 5:52 PM
NCT ID:
NCT06986668
Eligibility Criteria:
Inclusion Criteria:
* Being between the ages of 18-65
* Agreeing to participate voluntarily in the study
* Being diagnosed with mild or moderate idiopathic chronic CTS as a result of anamnesis, clinical examination and nerve conduction study
Exclusion Criteria:
* Presence of predisposing etiological factors for CTS such as diabetes mellitus, chronic kidney and liver disease, acromegaly, rheumatological diseases, acute trauma, hypothyroidism, etc.
* Being diagnosed with severe CTS
* Having a history of previous wrist surgery or trauma
* Having atrophy in the thenar region or weakness in the thenar muscles
* Having cervical radiculopathy, thoracic outlet syndrome, polyneuropathy, brachial neuropathy or proximal median nerve neuropathy
* Having had steroid injections in the last 3 months and taking oral steroid medications
* Being pregnant
* Having an open wound or rash in the wrist and its surroundings that would prevent treatment
* Patients who are receiving or will receive another/additional treatment for CTS
* Patients with a bifid median nerve, persistent median artery, ganglion cyst, tenosynovitis, or tendinitis in the wrist.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT06986668
Study Brief:
Protocol Section:
NCT06986668