The purpose of this study is to determine optimal treatment strategies for symptomatic walled-off pancreatic necrosis( WON).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Patients will be stratified into two arms (Greater than 50% necrosis or less than 50% necrosis), then will be randomized to either the double pigtail plastic stent or AXIOS metal stent
Patients will be stratified into two arms (Greater than 50% necrosis or less than 50% necrosis), then will be randomized to either the double pigtail plastic stent or AXIOS metal stent
Complete resolution as defined by complete radiographic resolution of the walled-off necrosis (WON)
Time frame: Baseline to 4 months after initiation of endoscopic treatment
Clinical resolution of infection as defined by complete radiographic resolution and/or symptoms of pain and gastric outlet obstruction
Time frame: Baseline to 4 months after initiation of endoscopic treatment
Symptom resolution (Visual Analogue Scale for pain, gastric outlet obstruction, and weight gain)
Time frame: Baseline to 4 months after initiation of endoscopic treatment
Decrease in incidence of adverse events
Time frame: Baseline to 4 months after initiation of endoscopic treatment
Decrease in number of hospital days during treatment course
Time frame: Baseline to 4 months after initiation of endoscopic treatment
Decrease in total costs of pancreatitis-related health care during treatment course
Time frame: Baseline to 4 months after initiation of endoscopic treatment
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