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
| Type | Name | Description |
|---|---|---|
| DRUG | Rectal indomethacin 100mg one time before or after ERCP | Patients 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.