The aim of this study is to determine the average patency period of the new anti-reflux biliary stent on patients with malignant bile duct strictures and to determine if this stent remains patent for a longer period of time comparing with the ordinary plastic Tannenbaum biliary stent.
Bile duct related cancer is a condition quite commonly seen among Asians. Predisposing conditions for primary bile duct cancer include recurrent infections and autoimmune diseases such as recurrent pyogenic cholangitis (RPC) and primary sclerosing cholangitis (PSC) as well as congenital problem such as choledochal cyst. Peri-ampullary tumour, pancreatic tumour and metastatic tumours with bile duct compression are other causes of bile duct obstruction. As many of these tumours are discovered at a late stage, curative treatment is usually not feasible. Palliative endoscopic stenting of the obstructed biliary system remains the treatment of choice for the majority. The main problem with endoscopic stenting of the biliary system is the short stent patency period. There are some reports on modifications to plastic biliary stenting method in recent years including changes in stent designs, use of a different material or coating, administrating prophylactic antibiotics and the use of special drugs. All these have failed to show any conclusive effect on the stent patency period. A preliminary study has demonstrated some promising results in the use of a stent with an anti-reflux property very similar to the stents the investigators are using in this study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
16
Anti-reflux Tannenbaum biliary stent
Ordinary Tannenbaum biliary stent
Endoscopy Centre
Hong Kong, China
time-to-occlusion or stent patency period in days
Time frame: within 25 weeks of device application
Bleeding associated with endoscopic retrograde cholangiopancreatography (ERCP) and stent placement
Time frame: within 25 weeks of device application
perforation associated with ERCP and stent placement
Time frame: within 25 weeks of device application
pancreatitis associated with ERCP and stent placement
Time frame: within 25 weeks of device application
cholangitis associated with ERCP and stent placement
Time frame: within 25 weeks of device application
stent migration associated with ERCP and stent placement
Time frame: within 25 weeks of device application
all cause mortality
Time frame: within 25 weeks of device application
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