Adverse events associated with ERCP for biliary diseases; a prospective multicenter observational study.
Not Applicable
- Conditions
- Adverse events associated with ERCP
- Registration Number
- JPRN-UMIN000024820
- Lead Sponsor
- Bilio-Pancreatic Stenting study group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 3739
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients with clinical evidence of acute pancreatitis at the time of the procedure. 2) Patients with altered gastrointestinal anatomy. e.g. Roux-en-Y reconstruction. 3) Patients whose ASA performance status is more than 3.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence and severity of adverse events associated with ERCP.
- Secondary Outcome Measures
Name Time Method 1)Risk factors for post-ERCP pancreatitis. 2)Effectiveness of preventive procedures for post-ERCP pancreatitis.