Prevention of Acute Pancreatitis after examination of the bile ducts using only guidewire versus guidewire and contrast
Not Applicable
Recruiting
- Conditions
- acute pancreatitisC06.689.750
- Registration Number
- RBR-979wh3
- Lead Sponsor
- niversidade Federal de Ciências da Saúde de Porto Alegre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Consecutive patients over 18 years of age who are referred to the Radiology Center of the São José Pavilion (Biliary Endoscopy Service of Santa Casa / UFCSPA) will be included to perform CPER that, after due explanations about the study, agree to participate and sign the term of free and informed consent.
Exclusion Criteria
Patients who: have previously undergone endoscopic retrograde cholangiopancreatography, refuse to participate, and those whose ERCP is performed during the course of acute pancreatitis will be excluded from the study.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post ERCP pancreatitis incidence, measured by the number of patients who developed acute pancreatitis after ERCP - acute pancreatitis will be considered typical abdominal pain associated with increased blood levels of amylase or lipase levels by at least 3 times the upper limit of normality, and / or characteristic radiological image of acute pancreatitis.
- Secondary Outcome Measures
Name Time Method cannulation rate of the bile duct, measured by the number of times that the biliary way could be cannulated.;procedure time, measured in minutes.;pre-cut rate, measured in the number of times the pre-cut technique had to be performed to cannulate the bile duct.