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Scalpel Versus Electrocautery for Surgical Skin Incision in Open Carpal Tunnel Release

Scalpel Versus Electrocautery for Surgical Skin Incision in Open Carpal Tunnel Release - Randomized, Controlled Open-Label Trial

Status
Terminated
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02791529
Acronym
OCTR-Electro
Enrollment
16
Registered
2016-06-06
Start date
2016-09-30
Completion date
2018-01-31
Last updated
2020-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome

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).

Interventions

Skin incision performed by electrocautery

PROCEDUREScalpel

Skin incision performed by scalpel

Sponsors

Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Pain on visual analogue scaleFirst postoperative day

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026