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Clinical Trial Summary

The primary aim of this study is to collect clinical data on the performance of MonoPlus® suture applied in routine clinical practice. Diverse parameters are to be used to assess the safety and efficacy of MonoPlus® suture for gastrointestinal anastomosis construction. This study has been designed to implement an action within the framework of a proactive Post Market Clinical Follow up (PMCF) activity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04811833
Study type Observational
Source Aesculap AG
Contact
Status Withdrawn
Phase
Start date July 2022
Completion date December 2023

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