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Clinical Trial Summary

The aim of this non-interventional study is to evaluate the efficacy of a monofilament, mid-term absorbable suture material (Monosyn®) for anastomosis performed in the gastrointestinal tract using the frequency of anastomosis leakage as a primary parameter.

Postoperative complication rate, length of hospital stay, costs, time to perform the anastomosis and handling will serve as secondary endpoints.

The question is addressed, whether a monofilament suture material is as effective as a braided suture material for anastomosis construction within the gastrointestinal tract.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02080702
Study type Observational
Source Aesculap AG
Contact
Status Terminated
Phase
Start date August 2014
Completion date June 2016

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