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Performance of Safety of SILKAM® Suture Material in Oral Surgery — SILKOS  

Tooth, Impacted Clinical Trial

Official title:
Single Center Open-Label Post Market Clinical Follow-Up (PMCF) -Study on the Performance of Safety of SILKAM® Suture Material in Oral Surgery

Clinical Trial Summary

Assessment of SILKAM® suture material in mucosal closure in oral surgery (mucosal sutures). A prospective, monocentric, single arm observational study.

Clinical Trial Description

The aim of this Non Interventional Study is to collect systematically and proactively different clinical parameters regarding safety, effectiveness, and performance of SILKAM® suture material under the daily routine clinical practice when is intended to be used for oral surgery. All patients enrolled will be prospectively followed until suture removal, which takes place approximately one week post-operatively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05296902
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date September 21, 2022
Completion date November 16, 2023
View Details
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