Trials / Completed
CompletedNCT00433771
A Study of the WallFlex™ Biliary Fully-covered Stent for the Palliative Treatment of Malignant Bile Duct Obstruction
A Multi-Center, Single Arm, Prospective Study of the WallFlex™ Biliary Fully-covered Stent for the Palliative Treatment of Malignant Bile Duct Obstruction
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 74 (actual)
- Sponsor
- Boston Scientific Corporation · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | WallFlex™ Biliary Fully Covered Metal Stent placement | Implantable metal biliary stent intended for use in the palliative treatment of biliary strictures produced by malignant neoplasms. The stent is fully covered with a polymer to reduce the potential for tumor ingrowth into the stent. |
Timeline
- Start date
- 2007-03-01
- Primary completion
- 2008-05-01
- Completion
- 2008-05-01
- First posted
- 2007-02-12
- Last updated
- 2010-06-29
- Results posted
- 2010-02-09
Locations
10 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00433771. Inclusion in this directory is not an endorsement.