Scalpel Versus Electrocautery for Surgical Skin Incision in Open Carpal Tunnel Release
Phase 1
Terminated
- Conditions
- Carpal Tunnel Syndrome
- Interventions
- Procedure: ScalpelProcedure: Electrocautery
- Registration Number
- NCT02791529
- Lead Sponsor
- Turku University Hospital
- Brief Summary
The use of electrocautery for surgical skin incision in general surgery is known to decrease post-operative pain. This study compares the use of scalpel and electrocautery for surgical skin incision in open carpal tunnel release (OCTR).
- Detailed Description
The use of electrocautery for surgical skin incision in general surgery is known to decrease post-operative pain. This study compares the use of scalpel and electrocautery for surgical skin incision in open carpal tunnel release (OCTR).
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 16
Inclusion Criteria
- Age 18 - 60 years
- Scheduled to undergo open carpal tunnel release (OCTR) by a study group member
- Gives informed consent
- diagnosis of chronic carpal tunnel syndrome
Exclusion Criteria
- -Any current underlying systemic illness or condition that may affect wound healing (e.g. diabetes or chronic vascular disease)
- History of severe systemic or focal illness (e.g. previous myocardial infarction, chronic obstructive pulmonary disease)
- Chronic skin condition in the affected upper limb (e.g. psoriasis)
- Pregnancy
- Inability to comprehend the consent form (in Finnish) or inability to give consent
- Previous surgery or scar in the palmar aspect of the affected wrist
- Recurrent carpal tunnel syndrome
- Previous significant trauma of the affected upper extremity (including distal radius fracture) or suspicion of acute onset carpal tunnel syndrome
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Scalpel Scalpel Skin incision performed by scalpel Electrocautery Electrocautery Skin incision performed by electrocautery
- Primary Outcome Measures
Name Time Method Pain on visual analogue scale First postoperative day
- Secondary Outcome Measures
Name Time Method