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Performance of Novosyn® in Patients Undergoing Uterus Closure in Cesarean Section — SCOTT  

Cesarean Section Complications Clinical Trial

Official title:
Assessment on the Performance of Novosyn® in Patients Undergoing Uterus Closure in Cesarean Section. A Retrospective, Monocenter, Observational Study in Daily Practice

Clinical Trial Summary

The aim of this study is to collect clinical data on the use of Novosyn® applied for the uterus closure in cesarean section. Diverse parameters have been selected to assess that the safety and effectiveness of Novosyn® is comparable to published results, where the rate of SSIs in patients undergoing uterus closure in cesarean section was 10.6%.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05807633
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date June 15, 2022
Completion date October 1, 2023
View Details
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