SEAL Registry - European Registry for the Effectiveness of LifeSeal® Kit

Status Active, not recruiting

Clinical Trial Summary

This study will assess the effectiveness of commercially available LifeSeal® Kit as measured by the incidence of post-operative clinical anastomotic leak rates in subjects undergoing low and ultralow anterior resection with an anastomosis. All patients treated with LifeSeal® will be offered to participate

Clinical Trial Description

The LifeSeal® Kit is a novel surgical sealant intended to be used as an adjunct to suture or staple line during standard surgical repair of the GI tract (anastomosis or linear) to provide re-inforcement and help reduce leaks. The LifeSeal™ Kit has recently been CE certified on March 2016 for marketing in the European Union. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02881359
Study type	Observational [Patient Registry]
Source	LifeBond Ltd.
Contact
Status	Active, not recruiting
Phase
Start date	October 2016
Completion date	September 2018

View Details

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