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A study on the effectiveness of Indomethacin in preventing post Endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis

Among patients undergoing Endoscopic Retrograde Cholangiopancreatography (ERCP), does a single dose of Indomethacin reduce the incidence of Post-ERCP Pancreatitis?

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613000096752
Enrollment
600
Registered
2013-01-24
Start date
2013-02-20
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

We propose a randomised control study to assess the use of prophylactic Non-steroidal Anti-inflammatory Drugs for the prevention of Post Endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis.

Interventions

Indomethacin is a Non-Steroidal Anti-inflammatory Drug (NSAID), which is commonly used to treat fever, headaches, and bone, muscular or joint pain. It works by inhibiting the production of prostaglandins (known to cause such symptoms). It is marketed under several names, including Indocid and Arthrexin. In our study, participants will be given an Indomethacin suppository (dose given rectally) 5 minutes before the commencement of the ERCP. We will then be monitoring our patients for 90 minutes po

Indomethacin is a Non-Steroidal Anti-inflammatory Drug (NSAID), which is commonly used to treat fever, headaches, and bone, muscular or joint pain. It works by inhibiting the production of prostaglandins (known to cause such symptoms). It is marketed under several names, including Indocid and Arthrexin. In our study, participants will be given an Indomethacin suppository (dose given rectally) 5 minutes before the commencement of the ERCP. We will then be monitoring our patients for 90 minutes post procedure for symptoms, which would suggest pancreatitis (in particular abdominal pain).

Sponsors

Vinh-An Phan
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Caregiver)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All patients undergoing Endoscopic Retrograde Cholangiopancreatography

Exclusion criteria

-Those with active pancreatitis -Renal impairment -known allergy to non-steroidal anti-inflammatory drugs (including NSAID induced asthma) -patients with concomitant NSAID therapy (excluding Aspirin) -patients without a native papilla -Active peptic ulcer disease

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026