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 @ 12:36 PM
Ignite Modification Date:
2025-12-24 @ 12:36 PM
NCT ID:
NCT05904561
Eligibility Criteria:
Inclusion Criteria:
1. Postpartum women with mild to moderate carpal tunnel syndrome will participate in this study.
2. Their ages will range from 25 to 35 years old.
3. Their BMI will be ranged from 25 to 30 Kg/m2.
4. The electrophysiological evidence of mild or moderate median nerve lesion at wrist (mild: sensory nerve conduction velocity slow on finger/wrist measurement, sensory nerve latency \>3.5 ms, normal terminal motor latency; moderate: sensory potential preserved with motor slowing, distal motor latency to abductor pollicis brevis (APB) \< 6.5 ms) (Bland, 2000 and Dumitru and Zwarts, 2002).
5. Positive phalen's test.
6. Positive tinel's test.
7. Unilateral or bilateral carpal tunnel affection will be included.
Exclusion Criteria:
1. History of brachial plexopathy or malignancy.
2. Radial, ulnar neuropathy, proximal median neuropathy or polyneuropathy.
3. Previous wrist surgery or steroid injection for carpal tunnel syndrome.
4. History of trauma, fracture, deformity or inflammation in the wrist, such as rheumatoid arthritis.
5. Coagulation abnormalities, pregnancy, fever and infections.
6. Skin disease and skin cancer.
7. Spots, birthmarks or tattoos over the work points.
8. Pacemaker and implementable medical devices.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
25 Years
Maximum Age:
35 Years
Study:
NCT05904561
Study Brief:
Protocol Section:
NCT05904561