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Clinical Trial Summary

The purpose of the registry was to observe the safety and effectiveness outcomes for subjects treated with the EndoBarrier in the post market setting where the product had Conformité Européene (CE mark) regulatory approval and in accordance to the approved Indication For Use.


Clinical Trial Description

This was a worldwide observational registry of the use of the EndoBarrier for inclusion of subjects treated with the EndoBarrier in centers in Australia, Chile, and the Netherlands. The registry was open to all subjects at participating centers that received the EndoBarrier. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03072901
Study type Observational [Patient Registry]
Source GI Dynamics
Contact
Status Terminated
Phase N/A
Start date December 2010
Completion date February 2016

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