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Clinical Trials/NL-OMON30737
NL-OMON30737
Not yet recruiting
Not Applicable

A multi-center, single arm, prospective study of the WallFlex biliary partially covered stent for the palliative treatment of malignant bile duct obstruction. - WallFlex Biliary PC Study

Boston Scientific Corporation0 sites18 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malignant biliary obstruction
Sponsor
Boston Scientific Corporation
Enrollment
18
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Inoperable extrahepatic biliary obstruction by any malignant process.
  • Indicated for metal stent placement for palliative treatment of biliary stricture(s) produced by malignant neoplasms.

Exclusion Criteria

  • Strictures that cannot be dilated enough to pass the delivery system.
  • Perforation of any duct within the biliary tree.
  • Presence of metal biliary stent.
  • Patients with active hepatitis.

Outcomes

Primary Outcomes

Not specified

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