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Study identifier: NCT05267379 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

An European Multi-centre Cohort Study for Unravelling Pharmacokinetic and Genetic Factors Underlying Post-ERCP Pancreatitis

Condition: Post-ERCP Acute Pancreatitis  ·  Sponsor: Radboud University Medical Center

PhaseN/A
Planned participants700
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Endoscopic retrograde cholangiopancreatography (ERCP) comes with a risk for post-ERCP pancreatitis (PEP), which accounts for considerable morbidity, high healthcare expenditure, and death. The pathophysiology of PEP and the underpinnings of the preventive effect of rectal NSAID (RN) is poorly understood. Guidelines advise to take preventive measures with a single dose of 100mg RN, peri-ERCP. While NSAID administration reduces the risk with 40%, PEP still occurs after ERCP. In addition, patients with a PEP history have a higher risk to develop recurrence after a subsequent ERCP. This might suggest that an underlying genetic risk may contribute to increasing the incidence of PEP in some patients.

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

Talk to the study team

Mike de Jong, MD  ·  0031883207054  ·  mike.dejong@radboudumc.nl

Always discuss trial participation with your own doctor first.

Locations (1)

RadboudUMCNijmegen, Gelderland, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT05267379