The effect of drain application on outcome of surgery
Not Applicable
Recruiting
- Conditions
- Carpal Tunnel Syndrome.Carpal tunnel syndrome
- Registration Number
- IRCT20161225031559N3
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 62
Inclusion Criteria
Patients with severe carpal tunnel syndrome confirmed by clinical examination and electrodiagnostic testing.
Patients with Moderate carpal tunnel syndrome who did not respond to conservative treatment
Informed consent
Exclusion Criteria
Patients who simultaneously undergo surgery in addition to releasing the carpal tunnel.
Patients with intraoperative Iatrogenic vascular injury
Patients with a history of anticoagulation therapy Or coagulation disorders.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The extent of bleeding and hematoma. Timepoint: 2 days after surgery. Method of measurement: The extent of bleeding on the dressing gauze and Expert examination.
- Secondary Outcome Measures
Name Time Method Postoperative pain. Timepoint: 2, 4 and 6 weeks after surgery. Method of measurement: The visual analogue scale.;Pinch strength. Timepoint: 2, 4, 6 months after surgery. Method of measurement: Pinch meter.