NCT01343160

Removable GORE VIABIL® Biliary Endoprosthesis for Treatment of Benign Biliary Strictures

Multicenter Study of Removable GORE VIABIL® Biliary Endoprosthesis for Treatment of Benign Biliary Strictures

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 43 (actual)
• Sponsor: W.L.Gore & Associates · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to generate clinical data to support the use of GORE® VIABIL® Biliary Endoprosthesis in the endoscopic and percutaneous treatment of benign biliary strictures.

Conditions

• Biliary Strictures

Interventions

Type	Name	Description
DEVICE	GORE® VIABIL® Biliary Endoprosthesis	Deployment of GORE® VIABIL® Biliary Endoprosthesis to the area of stricture

Timeline

• Start date: 2011-04-01
• Primary completion: 2015-05-01
• Completion: 2015-05-01
• First posted: 2011-04-27
• Last updated: 2021-04-21
• Results posted: 2021-04-21

Locations

1 site across 1 country: Germany