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Randomised Trial Comparing Metal and Plastic Biliary Stents Stents for Palliating Malignant Jaundice

Primary Purpose

Biliary Obstruction

Status
Unknown status
Phase
Phase 4
Locations
South Africa
Study Type
Interventional
Intervention
SEMS
Sponsored by
University of Cape Town
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Biliary Obstruction focused on measuring biliary, obstruction, malignant, stent, palliation

Eligibility Criteria

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

Inclusion Criteria:

  • Symptomatic jaundice secondary to malignant distal CBD stricture
  • Contra-indication to resection (advanced disease/advanced age/poor surgical risk)

Exclusion Criteria:

  • Hilar/proximal CBD obstruction
  • ECOG performance status 3 or 4
  • Duodenal obstruction
  • Previous stent placement
  • Inability to comply with follow-up
  • Ascites and liver metastases
  • Not possible to stent endoscopically

Sites / Locations

  • Groote Schuur HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

SEMS

Plastic stent

Arm Description

Self expanding metal stent compared to plastic stent. Both recognised forms of treatment for condition

Outcomes

Primary Outcome Measures

Overall cost comparison of metal versus plastic stent in patients with limited life expectancy

Secondary Outcome Measures

Quality of life assessment

Full Information

First Posted
August 5, 2008
Last Updated
August 5, 2008
Sponsor
University of Cape Town
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1. Study Identification

Unique Protocol Identification Number
NCT00731419
Brief Title
Randomised Trial Comparing Metal and Plastic Biliary Stents Stents for Palliating Malignant Jaundice
Official Title
Distal Malignant Biliary Obstruction: A Prospective Randomised Trial Comparing Metal and Plastic Stents in Palliation of Symptomatic Jaundice
Study Type
Interventional

2. Study Status

Record Verification Date
May 2007
Overall Recruitment Status
Unknown status
Study Start Date
June 2007 (undefined)
Primary Completion Date
May 2009 (Anticipated)
Study Completion Date
August 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Cape Town

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: When considering any malignancy with limited life expectancy, palliation and quality of life are paramount. Owing to the limited centres offering ERCP and endoscopic palliation in the South African state sector, patients often travel vast distances and spend large amounts of time away from family and social support structures, severely impairing their quality of life. Stent occlusion with resultant readmission to an ERCP accredited centre obviously compounds this problem. The hypothesis we propose to test is whether metal stents as a primary procedure result in better patency rates, are more cost effective and improve quality of life than plastic stents. We propose to do this by means of a randomised trial determining the best method of palliation for inoperable distal common bile duct malignancies in the South African context. Primary end-point Assessing the cost of metal versus plastic stenting in inoperable malignant distal common bile duct strictures in patients with expected survival of 3 months or more as palliation of symptomatic obstructive jaundice. Cost to be assessed in terms of hardware, hospital stay and readmissions for stent occlusion(patency) and complications Secondary end-point Assessing quality of life using a validated scoring system(EORTC QLQ 30) in patients receiving a metal or plastic biliary stent as definitive means of palliation of malignant obstructive jaundice Hypothesis to be tested Metal stents are superior to plastic stents in terms of patency, resulting in more cost effective palliation of inoperable malignant jaundice and better quality of life due to fewer stent occlusions/episodes of cholangitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biliary Obstruction
Keywords
biliary, obstruction, malignant, stent, palliation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
SEMS
Arm Type
Active Comparator
Arm Description
Self expanding metal stent compared to plastic stent. Both recognised forms of treatment for condition
Arm Title
Plastic stent
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
SEMS
Other Intervention Name(s)
Boston Scientific, biliary self-expanding metal stent, olympus plastic stent
Intervention Description
Comparing plastic and metal stents
Primary Outcome Measure Information:
Title
Overall cost comparison of metal versus plastic stent in patients with limited life expectancy
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Quality of life assessment
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptomatic jaundice secondary to malignant distal CBD stricture Contra-indication to resection (advanced disease/advanced age/poor surgical risk) Exclusion Criteria: Hilar/proximal CBD obstruction ECOG performance status 3 or 4 Duodenal obstruction Previous stent placement Inability to comply with follow-up Ascites and liver metastases Not possible to stent endoscopically
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
John M Shaw, FCS, MMed
Phone
021-404-3042
Email
John.Shaw@uct.ac.za
First Name & Middle Initial & Last Name or Official Title & Degree
Jake E Krige, FCS, FACS
Phone
021-404-3072
Email
Jake@curie.uct.ac.za
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John M Shaw, FCS, MMed
Organizational Affiliation
University of Cape Town
Official's Role
Principal Investigator
Facility Information:
Facility Name
Groote Schuur Hospital
City
Cape Town
State/Province
Western Cape
ZIP/Postal Code
7925
Country
South Africa
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John M Sahw, MBBCh, FCS
Phone
021-404-3042
Email
John.Shaw@uct.ac.za
First Name & Middle Initial & Last Name & Degree
John M Shaw, MBBCH,FCS

12. IPD Sharing Statement

Learn more about this trial

Randomised Trial Comparing Metal and Plastic Biliary Stents Stents for Palliating Malignant Jaundice

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