Hilar Cholangiocarcinoma Clinical Trial
Official title:
Efficacy and Cost Analysis of Plastic Stent Compare to Metallic Stent in Unresectable Complex Hilar Cholangiocarcinoma; a Randomized Controlled Trial
The purpose of this study is to compare the adequacy of unilateral endoscopic biliary drainage using metallic stent with plastic stent in unresectable, complex, hilar, cholangiocarcinoma and cost analysis.
There are two types of biliary stents: 1) the plastic stent made from polyethylene or
polytetrafluoroethylene; and, 2) the metal stent braided in the form of a tubular mesh from
surgical-grade stainless steel alloy and designed to expand to a maximum diameter of 10 mm.
The main drawback of the plastic stent is the relatively high occlusion rate, but its
advantage is the lower cost. The use of a metal stent for hilar tumor has many theoretical
advantages: 1) the flexible open-mesh design should allow drainage of secondary duct
branches; and, 2) its larger diameter may provide better drainage and longer patency (~3-9
months).
Whether one type of stent is superior in terms of adequacy of drainage or cost-effectiveness
remains undefined. Therefore, we would conduct this study to assess the efficacy of drainage
of endoscopically-inserted, unilateral, plastic stents vs. metallic stents in unresectable,
complex, hilar cholangiocarcinoma patients.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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