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 @ 6:47 PM
Ignite Modification Date:
2025-12-24 @ 6:47 PM
NCT ID:
NCT06940557
Eligibility Criteria:
Inclusion Criteria:
* all patients with numbness and tingling sensation at the first finger until the radial site of the 4th finger
* and/or fulfil the electrodiagnostic criteria of mild to moderate CTS, based on the Padua Scale as defined below:
* Mild: abnormal digit/wrist Sensory Nerve Conduction Velocity (CV) and normal Distal Motor Latency (DML)
* Moderate: abnormal digit/wrist Sensory Nerve Conduction Velocity (SNCV) and abnormal Distal Motor Latency (DML).
Exclusion Criteria:
* pregnant or breastfeeding women
* patients with symptoms of CTS but have normal NCS
* patients taking traditional or complementary medication for CTS
* patients with electrodiagnostic criteria of severe or extreme CTS as defined in the Padua scale:
* Severe: Absence of sensory response (SNAP) and abnormal Distal Motor Latency (DML).
* Extreme: Absence of motor (CMAP) and sensory responses (SNAP).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06940557
Study Brief:
Protocol Section:
NCT06940557