Double Incision and Comparison of the outcomes of Minimal Incision technique in treatment of carpal tunnel syndrome
Not Applicable
Recruiting
- Conditions
- Carpal tunnel syndrome.Carpal tunnel syndrome
- Registration Number
- IRCT20160508027797N5
- Lead Sponsor
- Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Patients with carpal tunnel syndrome
Exclusion Criteria
Failure to follow the patient after surgery
Carpal tunnel syndrome recurs after CTR surgery
Patients whose symptoms are severe, such as trauma, fracture, bleeding, and damage during surgery.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before surgery and six month of surgery. Method of measurement: Visual Analogue Scale.;Paresthesia. Timepoint: Before surgery and six month of surgery. Method of measurement: Based on patient response.;Numbness. Timepoint: Before surgery and six month of surgery. Method of measurement: Based on boston form.;Weakness. Timepoint: Before surgery and six month of surgery. Method of measurement: Based on boston form.
- Secondary Outcome Measures
Name Time Method Return to daily activities. Timepoint: Before surgery and six month of surgery. Method of measurement: Based on boston form.