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

Recruiting Observational Study
Pancreatitis, Acute ERCP Prophylaxis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
Branislav Kuncak · Other
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About This Trial
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 proced…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * ERCP in a patient with a native papilla (first ERCP) or repeat ERCP in a patient with previous failed cannulation attempt. * Age at least 18 years at the time of ERCP. * Signed informed consent. Exclusion Criteria: * Previous papillotomy, papilla dilation, or sphincteroplast…
Contacts

Branislav Kuncak, MD

+421232611113

branislav.kuncak@nsmas.sk

CONTACT

Rastislav Hustak, MD, Ph.D

+421335938810

rastislav.hustak@fntt.sk

CONTACT