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Study identifier: NCT07244432 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-ERCP Pancreatitis - Prophylactic Measures Implementation Study (PEP-PROMIS)

Condition: Pancreatitis, Acute · ERCP · Prophylaxis  ·  Sponsor: Branislav Kuncak

PhaseN/A
Planned participants1000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective, observational (non-interventional), multicenter study that will look at how often inflammation of the pancreas (called post-ERCP pancreatitis, or PEP) occurs after an endoscopic procedure known as ERCP. The study will take place in several hospitals in Slovakia and Czechia and will include all patients who have this procedure during the study period. ERCP is a common procedure used to treat problems in the bile ducts and pancreas. Although generally safe, it sometimes leads to PEP, which is the most frequent and potentially serious complication. Monitoring the rate of PEP helps doctors evaluate the overall quality of ERCP procedures, since patient safety is an important part of quality care. The study will also look at how well hospitals follow current prevention guidelines from two major professional organizations-the European Society of Gastrointestinal Endoscopy (ESGE) and the American Society for Gastrointestinal Endoscopy (ASGE)-and how these prevention methods affect the risk of PEP. This information will help identify how closely real-world practice follows recommended preventive measures and provide new data about PEP rates in the region.

This description comes directly from the study's public registry record.

Talk to the study team

Branislav Kuncak, MD  ·  +421232611113  ·  branislav.kuncak@nsmas.sk

Rastislav Hustak, MD, Ph.D  ·  +421335938810  ·  rastislav.hustak@fntt.sk

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital - St. Michael's Hospital, BratislavaBratislava, SlovakiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07244432