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:
2025-12-25 @ 1:07 AM
Ignite Modification Date:
2025-12-25 @ 1:07 AM
NCT ID:
NCT06912893
Eligibility Criteria:
Inclusion Criteria:
* Patients of all genders
* aged above 18 years
* suffering from mild to moderate carpal tunnel syndrome with typical symptoms like pain, paresthesia, or fine motoric disorders:
* very mild (grade 1): sensory nerve conduction velocity mildly reduced orslowercompared to the contralateral side.
* mild (grade 2): distal motor latency \<4,5ms and sensory nerve conduction velocity \< 40 m/s
* moderate (grade 3): distal motor latency between 4,5 and 6,5 ms and preserved sensory nerve amplitude.
* Patients with bilateral CTS also will be included, whereas the less symptomatic hand will be assessed as well, but receive no therapy.
Exclusion Criteria:
* Patients with severe CTS (distal motor latency above 6,5ms or absent sensory potentials);
* Prior therapy (even night splints) for CTS within the last six months
* The presence of common systemic diseases, that have known influence on the peripheral nerve system, like diabetes mellitus, polyneuropathy orabusive C2 consumption
* Postsurgical CTS
* Patients with serious injury of the wrist in medical history (e.g. radius fracture) or previous damage to median nerve and more proximal located compression syndrome of median nerve
* Patients with implanted electronic devices like defibrillators or pacemakers
* Pregnant women
* bifid median nerve;
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT06912893
Study Brief:
Protocol Section:
NCT06912893