Preoperative Biliary Drainage With Metal Versus Plastic Stents in Periampullary Cancer
Jaundice, Periampullary Cancer
About this trial
This is an interventional treatment trial for Jaundice focused on measuring ERCP, stent, preoperative biliary drainage
Eligibility Criteria
Inclusion Criteria:
A. Patients 20-80 years old B. Patients with surgically resectable periampullary cancer on CT scans with or without MRI or PET-CT scans C. ECOG Performance score 0 or 1 D. Patients who need preoperative biliary drainage (PBD) because of one or more of following causes
- Cholangitis defined as revised Tokyo guidelines
- Level of total bilirubin >= 10mg/dL
- Expected time to operation >= 7 days
Exclusion Criteria:
A. Patients who received previous endoscopic biliary drainage or percutaneous biliary drainage B. Patients with acute pancreatitis before PBD
C. Patients with bleeding tendency or coagulopathy or anticoagulation therapy as follows:
- Patients who take clopidogrel within 5 days before PBD
- Patients who take warfarin within 2 days before PBD
- Patients who receive heparin within 1 days before PBD D. Patients with pregnancy or suspected pregnancy E. Patients who are currently enrolled in another investigational trials that would directly interfere with current study
Sites / Locations
- Seoul National University Bundang Hospital
- Gachon University Gil Medical Center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Plastic stent
Uncovered metal stent
10 Fr plastic stent (Percuflex Amsterdam® or C-flex pigtail® or Advanix® Biliary stent)
Uncovered metal stent (WallFlex® Biliary RX stent)