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

Clinical Outcomes and Cost-Effectiveness of Waterproof Wound Closure Following Carpal Tunnel Decompression with Supplement 2-Octyl Cyanoacrylate Tissue Adhesive Versus Skin Suture plus Waterproof Wound Dressings: A Prospective Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221219005
Enrollment
62
Registered
2022-12-19
Start date
2021-12-01
Completion date
Unknown
Last updated
2026-08-03

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

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

Interventions

The wound was closed with 4-0 monofilament polypropylene (Prolene, Ethicon, US) plus waterproof occlusive dressing in the NSPWD group ,Wound closure was performed with a continuous subcuticular techni
Active Comparator Procedure/Surgery,Experimental Procedure/Surgery
non-absorbable sutures plus waterproof dressing (NSPWD) ,2-octyl cyanoacrylate tissue adhesive (2OCA)

Sponsors

NongKhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: adult patients who were clinically diagnosed as a carpal tunnel syndrome

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Wound-related cost 2- and 6-week postOp US dollar

Countries

Thailand

Contacts

Public ContactThodsaporn Maneesrisajja

Nongkhai hospital

t.meneesrisajja@gmail.com0894972391

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026