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Clinical Trial Summary

In this non-interventional study (NIS) a polyamide non-absorbable suture (Dafilon®) will be evaluated for skin closure in adult and pediatric patients. The aim of the study is to collect clinical data on the performance of Dafilon® for skin closure. The results of this study will generate further clinical evidence for the use and the benefit of a non-absorbable surgical suture material produced from polyamide. Furthermore, the proactive collection of clinical data for Dafilon® suture will support the maintenance of the suture material on the market, so that in the future other patients can receive the suture material for skin closure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04617041
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date March 11, 2021
Completion date June 15, 2023

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