Patency of a Prototype Large Plastic Biliary Stent in the Palliation of Malignant Distal Biliary Strictures.
Primary Purpose
Stricture, Obstruction, Cancer
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Large plastic biliary stent
Sponsored by
About this trial
This is an interventional treatment trial for Stricture focused on measuring obstruction, bile duct, malignant
Eligibility Criteria
Inclusion Criteria:
Inclusion Criteria:
- ≥ 18 and ≤ 85 years of age
- Malignant biliary obstruction, known or suspected
- Increased bilirubin or jaundice or history thereof
- Duct stricture (obstruction) ≥ 1 cm distal to the biliary hilum (bifurcation of the common hepatic duct into the right and left hepatic ducts)
- Not an operative candidate
Exclusion Criteria:
- Unable to obtain consent
- Unable to tolerate endoscopic procedure
- Suspected non-malignant bile duct stricture
- Candidate for potentially curative surgical intervention
- Previous SEMS
- Previous bile duct surgery
- Diffuse liver metastasis
- Peritoneal metastasis by CT
- Presence of ascites
- Duodenal obstruction preventing passage of the duodenoscope to the level of the papilla
- Failure to cannulate bile duct during ERCP
- Karnofsky performance score < 40
Sites / Locations
- Mayo Clinic Rochester
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Pancreatic Cancer Patients
Arm Description
A large plastic biliary stent was placed in the bile duct.
Outcomes
Primary Outcome Measures
Large Plastic Biliary Stents Will Have a Longer Patency Time Than Conventionally Used 10 Fr Stents in Subjects as Compared to Well-known Published Historical Control Data.
Secondary Outcome Measures
Full Information
NCT ID
NCT01590394
First Posted
April 30, 2012
Last Updated
September 18, 2017
Sponsor
Mayo Clinic
Collaborators
Olympus America, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01590394
Brief Title
Patency of a Prototype Large Plastic Biliary Stent in the Palliation of Malignant Distal Biliary Strictures.
Official Title
Prospective Evaluation of Luminal Patency of a Prototype Large Plastic Biliary Stent in the Palliation of Malignant Distal Biliary Strictures.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Terminated
Why Stopped
Difficulty in enrolling subjects and transporting scope for sterilization
Study Start Date
September 2012 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
Collaborators
Olympus America, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Plastic biliary stents which are a new larger size will remain free of obstructions for a longer period of time than currently used 10 French stents in cancer in the common bile duct.
Detailed Description
Malignant obstruction of the extra-hepatic bile duct often leads to jaundice and pruritus and occasionally results in cholangitis and bacteremia. Pancreatic cancer accounts for a large proportion of patients presenting with malignant extra-hepatic biliary obstruction. Most pancreatic cancers are unresectable at presentation, and palliation, including biliary decompression, is often a goal of therapy. Over the last decade, biliary decompression with endoscopically-placed stents during endoscopic retrograde cholangiopancreatography (ERCP) has largely replaced surgical bilioenteric diversion. Biliary decompression via endoscopic stenting alleviates cholestatic symptoms and improves quality of life. When compared to surgery, endoscopically placed plastic stents result in decreased morbidity and a trend towards decreased 30 day mortality. However, surgery is associated with a lower risk of recurrent biliary obstruction.
Stent diameter is an important factor in determining duration of biliary luminal patency. All plastic biliary stents will ultimately occlude due to deposition of bacterial biofilm. The original plastic biliary stents were 7 French (Fr) in diameter, with a patency rate of about 4 weeks. With increases in the size of the working channel of duodenoscopes, the limiting factor in what diameter stent can be deployed, 10 Fr stents were developed, with patency rates of approximately 15 weeks (3-4 months). Until recently, the largest stent that could be deployed with the current endoscopic technology using a conventional duodenoscope of acceptable outer diameter was 11.5 Fr; the limited available data suggest that these stents do not offer more prolonged luminal patency interval compared to 10 Fr stents.
In the early 1990s, self-expandable metal stents (SEMS) became available for use in palliation of malignant biliary obstruction. Once deployed, SEMS achieve larger diameters than plastic stents, which results in a longer median patency interval of approximately six to eight months.[3, 6, 9-12] Although effective, metal stents are eight to ten times more costly than plastic stents.
Recently, a large working channel duodenoscope with an acceptable outer diameter has been developed. This prototype duodenoscope allows passage of larger stents, which the investigators have successfully placed in select cases using this prototype. This duodenoscope, manufactured by Olympus Medical Systems Corp., is FDA approved.
The investigators hypothesize that, with the substantially increased luminal diameter, larger plastic stents will provide more prolonged relief of obstructive jaundice in patients with malignant distal common bile duct strictures. If this proves to be true, larger plastic stents may constitute a cost-effective alternative to SEMS, especially in health care systems that cannot afford SEMS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stricture, Obstruction, Cancer
Keywords
obstruction, bile duct, malignant
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Pancreatic Cancer Patients
Arm Type
Experimental
Arm Description
A large plastic biliary stent was placed in the bile duct.
Intervention Type
Device
Intervention Name(s)
Large plastic biliary stent
Intervention Description
Stent placement for bile duct obstruction.
Primary Outcome Measure Information:
Title
Large Plastic Biliary Stents Will Have a Longer Patency Time Than Conventionally Used 10 Fr Stents in Subjects as Compared to Well-known Published Historical Control Data.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Inclusion Criteria:
≥ 18 and ≤ 85 years of age
Malignant biliary obstruction, known or suspected
Increased bilirubin or jaundice or history thereof
Duct stricture (obstruction) ≥ 1 cm distal to the biliary hilum (bifurcation of the common hepatic duct into the right and left hepatic ducts)
Not an operative candidate
Exclusion Criteria:
Unable to obtain consent
Unable to tolerate endoscopic procedure
Suspected non-malignant bile duct stricture
Candidate for potentially curative surgical intervention
Previous SEMS
Previous bile duct surgery
Diffuse liver metastasis
Peritoneal metastasis by CT
Presence of ascites
Duodenal obstruction preventing passage of the duodenoscope to the level of the papilla
Failure to cannulate bile duct during ERCP
Karnofsky performance score < 40
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher J Gostout, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Rochester
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Patency of a Prototype Large Plastic Biliary Stent in the Palliation of Malignant Distal Biliary Strictures.
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