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A prospective single blind randomized controlled trial of covered versus uncovered biliary metal stents for the management of distal malignant biliary obstruction.

Phase 3
Recruiting
Conditions
Distal malignant biliary obstraction
Registration Number
JPRN-UMIN000000738
Lead Sponsor
International Medical Center of Japan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
112
Inclusion Criteria

Not provided

Exclusion Criteria

1, Patients with severe dysfunction of liver, kidney, heart, or lung. 2, Patients who are estimated to die within two months. 3,Patients with history of insertion of biliay metal stents 4, Patients with history of surgery of the common bile ducts. 5, Patients with stenosis of the hepatic ducts or the intra hepatic bile ducts. 6, Patients with stenosis of the duodenum which prevent passage of foods.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of the duration of the stents patency
Secondary Outcome Measures
NameTimeMethod
comparison of the safty comparison of the cost
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