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Fully Covered SEMS Versus Partially Covered SEMS With Anti-migration System for Malignant Distal Biliary Obstruction

Primary Purpose

Biliary Tract Neoplasms

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
partially covered SEMS
fully covered SEMS
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Biliary Tract Neoplasms

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1.> 19years 2.malignant biliary obstruction, 2 cm distal to hilum 3.unsuitable for curative surgical resection owing to metastasis, locally advanced stage, high operation risk, or patient's refusal

Exclusion Criteria:

  • 1.history of biliary surgery except cholecystectomy 2.history of SEMS placement 3.coagulopathy (INR>1.5, Platelet<50000) 4.expected survival > 3 months based on Karnofsky performance score 5.duodenal stricture

Sites / Locations

  • Samsung Medical CencerRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

partially covered SEMS

fully covered SEMS

Arm Description

Deployment of Partially covered biliary self expandable metal stent

Deployment of Fully covered biliary self expandable metal stent

Outcomes

Primary Outcome Measures

duration of stent patency

Secondary Outcome Measures

overall survival
stent occlusion rate
stent related complication

Full Information

First Posted
September 30, 2014
Last Updated
February 10, 2015
Sponsor
Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02255669
Brief Title
Fully Covered SEMS Versus Partially Covered SEMS With Anti-migration System for Malignant Distal Biliary Obstruction
Official Title
Comparison Between Fully Covered and Partially Covered Self-expandable Metal Stents With Anti-migration System for Malignant Distal Biliary Obstruction
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2014 (undefined)
Primary Completion Date
October 2016 (Anticipated)
Study Completion Date
October 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Samsung Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the duration of stent patency between partially covered and fully covered SEMS for palliation of malignant distal bile duct obstruction.
Detailed Description
Endoscopic stent placement has been used as a principle palliative method in patients with unresectable distal malignancy biliary obstruction. It has been pivotal in providing relief from obstructive jaundice, improving the quality of life, and allowing the maintenance of chemotherapy. Although SEMSs have been reported to be superior to plastic stents in terms of stent patency, they still have some debatable issues ; in uncovered SEMS, stent occlusion due to epithelial hyperplasia and tumor ingrowth through the metal mesh is a frequent problem, whereas covered SEMSs are prone to migration. The aim of the current study is to compare the duration of stent patency between partially covered and fully covered SEMS as a primary objective, and investigate overall patient survival, stent occlusion rate, and incidence of adverse events including stent dysfunction as secondary objectives.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biliary Tract Neoplasms

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
106 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
partially covered SEMS
Arm Type
Active Comparator
Arm Description
Deployment of Partially covered biliary self expandable metal stent
Arm Title
fully covered SEMS
Arm Type
Active Comparator
Arm Description
Deployment of Fully covered biliary self expandable metal stent
Intervention Type
Device
Intervention Name(s)
partially covered SEMS
Other Intervention Name(s)
Insertion of partially covered SEMS (PCSEMS)
Intervention Description
Used for palliation of inoperable malignant distal bile duct obstruction.
Intervention Type
Device
Intervention Name(s)
fully covered SEMS
Other Intervention Name(s)
Insertion of fully covered SEMS (FCSEMS)
Intervention Description
Used for palliation of inoperable malignant distal bile duct obstruction.
Primary Outcome Measure Information:
Title
duration of stent patency
Time Frame
From the date of randomization until the date of first documented stent dysfunction, assessed upto 12 months
Secondary Outcome Measure Information:
Title
overall survival
Time Frame
From the date of randomization until the date of death from any cause, assessed upto 12 months
Title
stent occlusion rate
Time Frame
From the date of randomization until the date of first documented stent occlusion, assessed up to 12 months
Title
stent related complication
Time Frame
From the date of randomization until the date of first documented stent related complication, assessed up to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1.> 19years 2.malignant biliary obstruction, 2 cm distal to hilum 3.unsuitable for curative surgical resection owing to metastasis, locally advanced stage, high operation risk, or patient's refusal Exclusion Criteria: 1.history of biliary surgery except cholecystectomy 2.history of SEMS placement 3.coagulopathy (INR>1.5, Platelet<50000) 4.expected survival > 3 months based on Karnofsky performance score 5.duodenal stricture
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jong Kyun Lee, M.D., Ph.D.
Phone
82-2-3410-3409
Email
leejk@skku.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jong Kyun Lee, M.D., Ph.D.
Organizational Affiliation
Samsung Medical Cencer
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Cencer
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jong-Kyun Lee, M.D., Ph.D.
Phone
81-2-3410-3409
Email
jongk.lee@samsung.com

12. IPD Sharing Statement

Learn more about this trial

Fully Covered SEMS Versus Partially Covered SEMS With Anti-migration System for Malignant Distal Biliary Obstruction

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