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Tissue Adhesive versus Skin Suture plus Waterproof Wound Dressings for Carpal Tunnel Wound Closure: A Prospective Randomized Controlled Trial

Phase 2
Completed
Conditions
adult patients who were clinically diagnosed as a carpal tunnel syndrome
carpal tunnel decompression, carpal tunnel syndrome, 2-octyl cyanoacrylate tissue adhesive, wound closure, waterproof wound closure, clinical outcomes, cost-effectiveness, wound-related cost
Registration Number
TCTR20221219005
Lead Sponsor
ongKhai Hospital
Brief Summary

Our study revealed that the supplementary tissue adhesive to subcuticular wound closure following CTD could improve patient satisfaction in the early postoperative period, enhance rapid ADL recovery, and reduce total wound-related costs despite increasing initial medical expenses. A tissue adhesive combined with subcuticular wound closure can be a reliable and cost-effective choice for waterproof skin closure following CTD

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
60
Inclusion Criteria

adult patients who were clinically diagnosed as a carpal tunnel syndrome

Exclusion Criteria

Patients who had uncontrolled medical conditions or skin diseases that affect wound healing, other previous palmar surgeries, known allergy to suture materials, previous keloid or hypertrophic scarring, or concurrent steroid or chemotherapy treatment were excluded from this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
QuickDASH score 2- and 6-week postOp 0-10 points,Number of dressing changes 2- and 6-week postOp time,Pain VAS 2- and 6-week postOp 0-10 points,Cosmetic VAS 2- and 6-week postOp 0-10 points,Patient satisfaction VAS 2- and 6-week postOp 0-10 points
Secondary Outcome Measures
NameTimeMethod
Wound-related cost 2- and 6-week postOp US dollar
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