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Effect of splinting for carpal tunnel syndrome

Not Applicable
Conditions
carpal tunnel syndrome.
carpal tunnel syndrome
Registration Number
IRCT138903224157N1
Lead Sponsor
Isfahan University Of Medical Sciences, Vice Chancellery For Reasearch
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
24
Inclusion Criteria

Presence of CTS diagnosed clinically for at least one month prior to the study and electrophysiological evidence of median neuropathy
Exclusion criteria: pregnancy, previously treated by surgery, steroid injection, or any other treatments, presence of neck arthroses

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Median sensory peak latency. Timepoint: before intrevention and four weeks after intervention. Method of measurement: by medtronic electromyography, anti dromic, in millisecound.;Median sensory amplitude. Timepoint: before intrevention and four weeks after intervention. Method of measurement: by medtronic electromyography, anti dromic, in millimeter.;Median sensory nerve conduction velocity. Timepoint: before intrevention and four weeks after intervention. Method of measurement: by medtronic electromyography, anti dromic, in m/s.
Secondary Outcome Measures
NameTimeMethod
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