Clinical Trials Directory

Trials / Completed

CompletedNCT02111707

Timing of Indomethacin Administration for the Prevention of Post-ERCP Pancreatitis (PEP)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
534 (actual)
Sponsor
University of Alberta · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To determine if the timing of administration of indomethacin affects the primary outcome of post-ERCP pancreatitis (PEP). Patients undergoing ERCP will be randomly assigned to receive pre or post-procedure rectal indomethacin to prevent the occurrence of PEP.

Conditions

Interventions

TypeNameDescription
DRUGRectal indomethacin 100mg one time before or after ERCPPatients will receive rectal indomethacin suppository 30 minutes before or immediately after ERCP for prevention of post-procedure pancreatitis. Patients will be randomized to the timing of administration.

Timeline

Start date
2014-04-01
Primary completion
2017-09-01
Completion
2017-09-01
First posted
2014-04-11
Last updated
2017-10-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02111707. Inclusion in this directory is not an endorsement.