Endoscopic Biliary RFA of Malignant Bile Duct Obstruction
Cholangiocarcinoma, Bile Duct Obstruction
About this trial
This is an interventional treatment trial for Cholangiocarcinoma
Eligibility Criteria
Inclusion Criteria:
- Histologically (preferred) or radiologically confirmed distal malignant bile duct tumors
- Inoperability by staging, comorbidities or patient wishes
Exclusion Criteria:
- History of bleeding disorder or use of anticoagulation
- prior cardiac pacemaker placement
- Presence of serious dysfunction of heart, lung or kidney.
- Presence of other malignancy
- Pregnancy
- Prior SEMS placement
- Prior Billroth II or roux-en Y reconstruction
Sites / Locations
- Medical Center for Digestive Diseases, The Second Affiliated Hospital of Nanjing Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
SEMS alone
SEMS plus radiofrequency ablation
Endoscopic retrograde cholangiopancreatography (ERCP) was performed under standard operating conditions with a duodenoscope (TJF 260V, Olympus, Tokyo, Japan) to confirm the length of the biliary stricture, diameter, and position. An uncovered self expanding metallic stent (SEMS) (Wallstent, Boston Scientific, USA) would be placed across the biliary stricture.
Endoscopic retrograde cholangiopancreatography (ERCP) would be performed under standard operating conditions to confirm the length of the biliary stricture, diameter, and position. The Habib EndoHBP catheter (Emcision, London, United Kingdom) was placed through the biliary stricture under fluoroscopic guidance. The RFA energy can be delivered repetitively at different tumor sites within one procedure, according to the stricture size. After the RFA application is completed, SEMS (Wallstent, Boston Scientific, USA) can be deployed.