Clinical Trials Directory

Trials / Completed

CompletedNCT02709421

Risk Factors of Post-ERCP Pancreatitis in Patients Receiving Rectal Indomethacin

Risk Factors Related to Post-endoscopic Retrograde Cholangiopancreatography Pancreatitis in High-risk Patients Who Underwent ERCP and Received Prophylactic Rectal Indomethacin

Status
Completed
Phase
Study type
Observational
Enrollment
790 (actual)
Sponsor
Air Force Military Medical University, China · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Post-endoscopic retrograde cholangiopancreatography(ERCP) pancreatitis (PEP)remains the most frequent adverse event of ERCP. Rectal indomethacin, as one kind of classic NSAIDs, has been proved to be effective in reducing the incidence of PEP. It has been widely used to prevent PEP in patients, especially those with potentially high risks of PEP. However, rectal indomethacin can not completely eradicate the occurrence of PEP. The rate of PEP in patients receiving indomethacin ranges from 3.2% to 9.2%. The risk factors of PEP in patients receiving rectal indomethacin remains unclear. The aim of the study was to identify potential risk factors in high-risk patients whose received administration of prophylactic rectal indomethacin after ERCP.

Conditions

Timeline

Start date
2016-02-01
Primary completion
2016-09-01
Completion
2016-09-01
First posted
2016-03-16
Last updated
2016-09-05

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT02709421. Inclusion in this directory is not an endorsement.