Clinical Trials Directory

Trials / Completed

CompletedNCT05747989

A Comparison of Tissue Adhesive Material and Suture as Wound-closure Techniques Following Carpal Tunnel Decompression

A Comparison of Tissue Adhesive Material and Suture as Wound-closure Techniques

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
98 (actual)
Sponsor
University of Split, School of Medicine · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Participants will be randomly assigned to suture-based wound closure (n=50) or tissue adhesive-based wound closure (n=50) with two-component skin adhesive Glubran Tiss 2®. The outcomes will be assessed during the follow-up period at intervals of 2, 6, and 12 weeks postoperatively. A scar assessment will be using the POSAS (Patient and Observer Scar Assessment Scale) and cosmetic VAS (Visual Analog Scale). The VNRS (Verbal Number Rating Scale) will used to assess pain.

Conditions

Interventions

TypeNameDescription
PROCEDUREtwo-component skin adhesive, Glubran Tiss 2After subcutaneous stitches a two-component skin adhesive, Glubran Tiss 2®, will be applied. G Each subject will receive 0.35 mL of Glubran Tiss® in the open wound, and before bandaging, subjects rested for 20 minutes for a polymerization process.
PROCEDUREskin is stitched with transcutaneous nylon suturesThe skin is stitched with transcutaneous nylon sutures (polypropylene-polyethylene monofilament, non-absorbable surgical suture) 4-0

Timeline

Start date
2022-06-01
Primary completion
2023-06-01
Completion
2023-08-01
First posted
2023-02-28
Last updated
2023-11-22

Locations

1 site across 1 country: Croatia

Source: ClinicalTrials.gov record NCT05747989. Inclusion in this directory is not an endorsement.