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Post-ERCP Pancreatitis Prevention by Stent Insertion

Not Applicable
Completed
Conditions
Post-ERCP Acute Pancreatitis
Registration Number
NCT01673763
Lead Sponsor
Technical University of Munich
Brief Summary

The presented study is designed to analyze the efficacy of pancreatic stent insertion in patients undergoing ERCP with accidental cannulation of the pancreatic duct.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
169
Inclusion Criteria
  • all patients undergoing ERCP with unintended cannulation or opifiacation of main pancreatic duct
  • age > 17 years
  • signed informed consent
Exclusion Criteria
  • intention to intervene main pancreatic duct
  • age < 18 years
  • pregnancy
  • absent of signed informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Incidence of post-ERCP pancreatitisup to 1 week
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

Deptartment of Hepatobiliary Diseases Leuven University Hospitals

🇧🇪

Leuven, Belgium

Klinikum rechts der Isar, Technische Universität München

🇩🇪

Munich, Germany

P. Stradin Clinical University Hospital Gastroenterology Centere Latvijas Universitates Medicinas

🇱🇻

Riga, Latvia

First city hospital of emergency care Northern State Medical University

🇷🇺

Arkhangelsk, Russian Federation

Deptartment of Hepatobiliary Diseases Leuven University Hospitals
🇧🇪Leuven, Belgium

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