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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of EUS-BD compared with ERCP-BD in low biliary obstruction caused by periampullary cancer, pancreatic cancer or low bile duct cancer. This is a single center, prospective, randomized-controlled study. The primary endpoint of this study is stent patency time, and secondary endpoints include technical success rate, clinical success rate, operation time, operation related complications rate, reintervention rate, stent patency rate at 6 months, and 1-year postoperative survival rate.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06196164
Study type Interventional
Source Peking Union Medical College Hospital
Contact Xi WU, M.D.
Phone 13683296860
Email wxpumch@163.com
Status Not yet recruiting
Phase N/A
Start date February 2024
Completion date December 2024

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