Biliary Obstruction Clinical Trial
Official title:
EUS-guided Biliary Drainage of First Intent With the Lumen Apposing Metal Stent vs. ERCP in the Management of Malignant Distal Biliary Obstruction: a Randomized Controlled Trial
NCT number | NCT03870386 |
Other study ID # | F11-36171 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 8, 2019 |
Est. completion date | July 1, 2023 |
Endoscopic ultrasound guided biliary drainage (EUS-BD) is an evolving field that has grown in popularity in the management of malignant biliary obstruction. Although Endoscopic retrograde cholangio-pancreatography (ERCP) with stent insertion has been the mainstay therapy throughout several decades, the transpapillary approach through tumor tissue is associated with significant risk for adverse events such as post-ERCP pancreatitis and stent dysfunction from tumor tissue overgrowth and ingrowth. EUS-BD, through the creation of a choledochoduodenostomy with a stent, has the potential advantage of avoiding the papilla and its associated complications while potentially improving stent patency with lower risks for tumor tissue ingrowth and/or overgrowth.
Status | Completed |
Enrollment | 144 |
Est. completion date | July 1, 2023 |
Est. primary completion date | May 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Radiological diagnosis (with or without pathological diagnosis) of borderline resectable, locally advanced, or unresectable malignant distal biliary obstruction at least 2 cm distal to the hilum. Resectability based on tumor staging on axial imaging and surgeon evaluation. - Elevated liver tests with serum bilirubin at least 3 times above the upper limit of normal (18.9 umol/L) - Dilated extra-hepatic bile duct measuring at least 1.2 cm on axial imaging or US - Confirmation of bile duct accessibility and size of at least 1.2 cm on endoscopic ultrasound - Karnofsky index > 30% - ASA score <IV - Provision of informed consent Exclusion Criteria: - Hilar obstruction (biliary obstruction < 2 cm from the hilum) - Uncorrectable coagulopathy and/or thrombocytopenia - Age < 18 - Liver metastasis involving > 30% of the liver volume - Liver cirrhosis with portal hypertension or ascites - Prior biliary sphincterotomy or stent placement - Surgically altered anatomy - Common bile duct measuring less than 1.2 cm will be excluded - Patient with clinical and radiological evidence of gastric outlet obstruction |
Country | Name | City | State |
---|---|---|---|
Canada | University of Calgary | Calgary | Alberta |
Canada | University of Alberta | Edmonton | Alberta |
Canada | Jewish General Hospital | Montreal | |
Canada | Centre Hospitalier Universite de Montreal | Montréal | Quebec |
Canada | Hopital Charles Lemoynes | Montréal | Quebec |
Canada | McGill University Health Centre | Montréal | Quebec |
Canada | The Ottawa Hospital | Ottawa | Ontario |
Canada | St-Michael's Hospital | Toronto | Ontario |
Canada | St-Paul Hospital | Vancouver | British Columbia |
Canada | Vancouver General Hospital | Vancouver | Bristish Columbia |
France | Hôpital Privé des Peupliers | Paris |
Lead Sponsor | Collaborator |
---|---|
McGill University Health Centre/Research Institute of the McGill University Health Centre |
Canada, France,
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* Note: There are 26 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of re-intervention | Obstruction and/or migration of stent | 1 year | |
Secondary | Technical success | successful insertion of a transpapillary stent or choledochoduodenostomy stent at the initial procedure at time of randomization | 1 year | |
Secondary | Clinical success | 50% decrease in bilirubin < 2 weeks post-stent insertion or less than 25% of pre-procedure bilirubin level within 4 weeks post stent insertion | 1 year | |
Secondary | Stent patency | mean time to stent obstruction or migration | 1 year | |
Secondary | Early adverse events | as per the ASGE lexicon for endoscopic adverse events13 including post-procedural pancreatitis defined as new or worsening abdominal pain persistent for at least 24 hours and requiring analgesics after ERCP or EUS-BD with an elevated amylase or lipase of greater than three times the upper limit of normal, peri-procedural bleeding defined as hematemesis and/or melena or hemoglobin drop > 2 g, intestinal perforation defined as evidence of air or luminal contents outside the GI tract, and cholangitis >38 Celsius for greater than 24 hours with cholestatic liver enzymes | 1 year |
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