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Optilene® Suture Material for Dermal Sutures — OPTIDERMAL  

Laceration Clinical Trial

Official title:
Assessment of Optilene® Suture Material for Skin Closure (Dermal Sutures). A Prospective Single-arm Observational Study in Daily Practice

Clinical Trial Summary

In this non-interventional study, Optilene® suture will be evaluated for skin closure in adult patients.

Clinical Trial Description

The study is designed as a prospective, unicentric and single-arm observational study to evaluate Optilene® suture material for skin closure. The product under investigation will be used in routine clinical practice and according to the Instructions for Use (IFU). After operation the investigator will examine the patients at discharge, at 10±5 days after surgery (removal of the suture) and 30±10 days postoperatively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05240248
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date June 22, 2022
Completion date July 23, 2023
View Details
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