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Clinical Trial Summary

The overall objective of this study is to assess the functionality of the WallFlex™ Biliary Fully-covered stent as a palliative treatment for malignant bile duct obstruction.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00433771
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase Phase 3
Start date March 2007
Completion date May 2008

See also
  Status Clinical Trial Phase
Completed NCT02103413 - EUS-guided Biliary Drainage Versus Percutanenous Transhepatic Biliary Darinage for Malignant Biliary Obstruction After Failed ERCP N/A
Completed NCT02114320 - Clinical Outcomes of EUS-guided Biliary Drainage Using Partially or Fully Covered Metallic Stents Phase 3
Completed NCT02197338 - Randomized Trial of Wire and Sphincterotome Systems for Biliary Cannulation N/A
Recruiting NCT04170933 - Magnetic Compression Anastomosis for Recanalization of Biliary Stricture N/A