Overview

Rectal Indomethacin to Prevent Post-Endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis

Status:
Terminated
Trial end date:
2014-12-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to assess whether peri-procedural administration of rectal indomethacin, compared to placebo, can reduce the incidence of post-ERCP pancreatitis.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Dartmouth-Hitchcock Medical Center
Treatments:
Indomethacin
Criteria
Inclusion Criteria:

1. Scheduled for an ERCP at Dartmouth-Hitchcock

2. Age greater than 18 years old

3. Ability to provide written informed consent

Exclusion Criteria:

1. Inability to provide written informed consent

2. ERCP being performed for diagnosis and/or treatment of acute pancreatitis

3. Current ongoing acute pancreatitis

4. Previously documented allergy to Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

5. Contra-indication to NSAID therapy (creatinine level >1.4 or active peptic ulcer
disease), already taking NSAIDs (other than aspirin therapy for cardioprotection)

6. Pregnant or nursing mothers