Prospective Evaluation of Winged Biliary Stent Patency in Patients With Benign Biliary Obstruction
Primary Purpose
Biliary Stricture
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Winged biliary stent (ViaDuct™)
Sponsored by
About this trial
This is an interventional treatment trial for Biliary Stricture
Eligibility Criteria
Inclusion Criteria:
All patients age 18 or older referred for ERCP for biliary obstruction from stones or benign strictures that have been confirmed based on clinical, laboratory and imaging findings, with an indication for plastic stent placement.
One or more biliary stents may be placed during the procedure depending on the indication such as a biliary stricture necessitating multiple stent placements for dilation as the standard of care.
- Expected patient survival of at least 90 days
- High likelihood of patient follow-up
- Patient is able to give a written informed consent
- Patient is willing and able to comply with the study procedures.
Exclusion Criteria:
- Patients with cholangitis
- Patients with bile leak
- Pregnant patients
- Patients with any contraindication to endoscopic procedure
- Participation in another investigational study that may directly or indirectly affect the results of this study within 30 days prior to the initial visit
- Patients with malignant biliary strictures
Sites / Locations
- Stanford University School of Medicine
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Winged stent
Arm Description
Placement of Winged stent for management of biliary obstruction. Stent to be placed for 90 days, with laboratory studies and clinical evaluation during this period to assess for stent potency.
Outcomes
Primary Outcome Measures
Count of Participants With Stent Patency at 90 Days
Evaluation of laboratory studies and clinical status to assess for stent patency/evidence of biliary obstruction
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03115411
Brief Title
Prospective Evaluation of Winged Biliary Stent Patency in Patients With Benign Biliary Obstruction
Official Title
Prospective Evaluation of Wing Biliary Stent Patency in Patients With Benign Biliary Obstruction
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
September 6, 2011 (Actual)
Primary Completion Date
April 10, 2018 (Actual)
Study Completion Date
April 10, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Evaluation of ERCP with placement of a winged plastic biliary stent without a lumen for management of benign biliary strictures.
Detailed Description
ERCP with plastic stent placement for resolution of biliary obstruction has been the method of choice for many years. However, stent obstruction is a major limitation of this approach. Studies have shown that the conventional tubular type polyethylene stents (CS) with side holes accumulate significant sludge and their mean patency is approximately 90 days.
Thus patients requiring longer term stenting need to undergo stent exchanges every 2-3 months.
Recently, a stent with a star-shaped cross-section has been developed for biliary applications. This FDA approved biliary Wing stent (WS) (ViaDuct™) is a novel plastic biliary stent that lacks a lumen, and is designed to allow bile to flow on the outside of the stent.
The stent which is star shaped in cross section, channels fluid along its winged perimeter.
It has been proposed that the winged stent design with a lack of central lumen obviates the risk of luminal occlusion and that the risk of occlusion, given the presence of multiple external drainage channels, is smaller. Longer term biliary drainage without the need for stent exchange should therefore be possible with these stents.
The primary aim of this study is to prospectively evaluate the patency rate of the winged stent in up to 90 days for patients with benign biliary obstruction.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biliary Stricture
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Patients with benign biliary obstruction who meet all inclusion criteria will be approached to consent for placement of a winged biliary stent for 90 days with appropriate laboratory studies and clinical evaluations.
Masking
None (Open Label)
Allocation
N/A
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Winged stent
Arm Type
Experimental
Arm Description
Placement of Winged stent for management of biliary obstruction. Stent to be placed for 90 days, with laboratory studies and clinical evaluation during this period to assess for stent potency.
Intervention Type
Device
Intervention Name(s)
Winged biliary stent (ViaDuct™)
Intervention Description
Placement of winged biliary stent at ERCP for management of benign biliary stricture.
Primary Outcome Measure Information:
Title
Count of Participants With Stent Patency at 90 Days
Description
Evaluation of laboratory studies and clinical status to assess for stent patency/evidence of biliary obstruction
Time Frame
90 days after placement of stent
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients age 18 or older referred for ERCP for biliary obstruction from stones or benign strictures that have been confirmed based on clinical, laboratory and imaging findings, with an indication for plastic stent placement.
One or more biliary stents may be placed during the procedure depending on the indication such as a biliary stricture necessitating multiple stent placements for dilation as the standard of care.
Expected patient survival of at least 90 days
High likelihood of patient follow-up
Patient is able to give a written informed consent
Patient is willing and able to comply with the study procedures.
Exclusion Criteria:
Patients with cholangitis
Patients with bile leak
Pregnant patients
Patients with any contraindication to endoscopic procedure
Participation in another investigational study that may directly or indirectly affect the results of this study within 30 days prior to the initial visit
Patients with malignant biliary strictures
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Prospective Evaluation of Winged Biliary Stent Patency in Patients With Benign Biliary Obstruction
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