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A randomized controlled trial comparing skin closure in limited open carpal tunnel release: Running subcuticular sutures versus Donati sutures.

Phase 4
Recruiting
Conditions
carpal tunnel syndrome
Carpal tunnel, scar, scar evaluation, POSAS, wound closure, VAS score, functional outcome
Registration Number
TCTR20191204002
Lead Sponsor
Faculty of Medicine, Prince of Songkla University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
141
Inclusion Criteria

All patients with carpal tunnel syndrome, based on the combination of patient's history (Pain, paresthesia and/or hypothesia in the hand in the area innervated by the median nerve), physical examination (thumb abduction weakness, thenar atrophy), and measurements of nerve conduction velocity. The patients age are range between 18 to 75 years, and have ability to complete the written inform consent. All of these patients who requires surgical decompression.

Exclusion Criteria

Exclusion criteria was included a history of lidocraine allergy, a history of wrist
trauma or previous operation, a history of underlying causes of CTS, such as diabetes mellitus, pregnancy, hypothyroidism, inflammatory arthropathy ,and obesity (body mass index (BMI) >30). Patient who had a history of hypertrophic scar and had past history of wound healing problem also excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
surgical scar 2 weeks, 6 weeks and 3 months after operation POSAS score
Secondary Outcome Measures
NameTimeMethod
VAS score and functional outcome 2 weeks, 6 weeks and 3 months after operation DASH score and VAS score
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