Comparison the results of surgical treatment for carpal tunnel syndrome in both the classical and minimal invasive Smillie knife
Not Applicable
- Conditions
- Carpal Tunnel Syndrom.Carpal tunnel syndrome
- Registration Number
- IRCT2015053110492N1
- Lead Sponsor
- kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 98
Inclusion Criteria
non-surgical treatment failure in patients with carpal tunnel syndrome; moderate and severe disease based on nerve-muscle strip .
Exclusion criteria: cervical radiculopathy; peripheral nerve lesions; old fractures of the forearm and wrist; congenital bone deformity of the upper limb; rheumatic diseases such as rheumatoid arthritis; minor clashes in the nerve strip ; neuropathy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before surgery, after five day,two week , six weeks, three and six month of surgery. Method of measurement: Based on patient response.;Paresthesia. Timepoint: Before surgery, after five day,two week , six weeks, three and six month of surgery. Method of measurement: Based on patient response.;Return to daily activities. Timepoint: Before surgery, after five day,two week , six weeks, three and six month of surgery. Method of measurement: Based on boston form.;Scar-site surgery. Timepoint: Five day,two week , six weeks, three and six month of surgery. Method of measurement: Based on surgeon observation.
- Secondary Outcome Measures
Name Time Method Wound infection. Timepoint: Five day,two week , six weeks, three and six month of surgery. Method of measurement: Surgeon observation.;Nerve injury. Timepoint: Six week after surgery. Method of measurement: Electrodiagnostic finding.