Carpal Tunnel Syndrome Clinical Trial
Official title:
Effect of Low Level Laser Therapy Versus Pulsed Ultrasound on Postpartum Carpal Tunnel Syndrome
Verified date | August 2023 |
Source | Egymedicalpedia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Carpal tunnel syndrome (CTs), the most common entrapment neuropathy of the upper extremity, is caused by compression of the median nerve as it travels through the carpal tunnel. CTs was clinically diagnosed in more than half of women (62%). Neurophysiological evaluation diagnosed that CTs in around half of women (43%) was positive in one hand at least, also, it was reported that about half of women with CTs during pregnancy still complained of CTs symptoms one year after delivery.
Status | Completed |
Enrollment | 48 |
Est. completion date | August 20, 2023 |
Est. primary completion date | August 1, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 25 Years to 35 Years |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Physical Therapy - Cairo University | Cairo |
Lead Sponsor | Collaborator |
---|---|
Egymedicalpedia |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain Intensity | measure pain intensity for each woman in all groups (A, B and C). The VAS is usually presented as a 10-cm horizontal line on which the patient's pain intensity is represented by a point between the extremes of "no pain at all" and "worst pain imaginable." Its simplicity, reliability and validity, as well as its ratio scale properties make the VAS the optimal tool for describing pain intensity | From base line to 4 weeks from starting the treatment |
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