Carpal Tunnel Syndrome Clinical Trial
Official title:
Effect of Different Doses of Therapeutic Ultrasound in the Treatment of Carpal Tunnel Syndrome
The purpose of this study will be to investigate the effective dose of therapeutic ultrasound in the treatment of carpal tunnel syndrome on pain level, functional ability, motor and sensory nerve conduction parameters and pinch strength.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | April 2024 |
Est. primary completion date | March 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years to 55 Years |
Eligibility | Inclusion Criteria: 1. Subject's age range will be 25-55 years . 2. Mild to moderate CTS, that is confirmed by neurologist or orthopedist based on results of physical examination and electrophysiological criteria; i. Mild CTS is characterized by sensory fibers involvement (sensory peak latency > 3.6 milliseconds) with no motor fiber involvement (motor distal latency < 4.1 milliseconds), provided that sensory nerve action potential (SNAP) is not absent. ii. Moderate CTS is characterized by involvement of both sensory and motor fibers, provided that neither of these two waves is absent . 3. Pain intensity more than 5 in visual analogue scale (VAS). Exclusion Criteria: 1. History of any trauma on the hands, neck, and shoulders within 3 months of the study onset 2. Cervical radiculopathy, peripheral polyneuropathy, or other neurological conditions. 3. Patients suffering from severe CTS according to electrophysiological criteria - |
Country | Name | City | State |
---|---|---|---|
Egypt | Ismailia Medical Complex | Ismailia |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | symptoms severity and functional status | symptoms severity and functional status will be measured by Boston carpal tunnel syndrome questionnaire,The patient will rate their ability to perform the activity on a scale that ranged from 1 (no difficulty with the activity) to 5 (cannot perform the activity at all). | four weeks following end of treatment | |
Primary | median nerve motor distal latency | Electrodiagnostic tests will be used to measure median nerve motor distal latency in milliseconds. | four weeks following end of treatment | |
Primary | median nerve motor amplitude | Electrodiagnostic tests will be used to measure motor amplitude in millivolt. | four weeks following end of treatment | |
Primary | median nerve sensory distal latency | Electrodiagnostic tests will be used to measure median nerve sensory distal latency in milliseconds. | four weeks following end of treatment | |
Primary | median nerve sensory amplitude | Electrodiagnostic tests will be used to measure sensory amplitude in millivolt | four weeks following end of treatment | |
Primary | pain intensity | pain intensity will be measured by visual analogue scale that is a straight line with one end meaning no pain and the other end meaning the worst pain imaginable,minimum score is best | four weeks following end of treatment | |
Primary | pinch strength | Pinch dynamometer will be used to measure pinch strength | four weeks following end of treatment |
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