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

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years

• written informed consent

• Indication to undergo an ERCP

Locations
Other Locations
Netherlands
RadboudUMC
RECRUITING
Nijmegen
Contact Information
Primary
Mike de Jong, MD
mike.dejong@radboudumc.nl
0031883207054
Time Frame
Start Date: 2022-03-01
Estimated Completion Date: 2027-12-01
Participants
Target number of participants: 700
Treatments
PEP patients
Patients who develop PEP
Control cohort
Patients who do not develop PEP
Sponsors
Leads: Radboud University Medical Center

This content was sourced from clinicaltrials.gov