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Low dose flurbiprofen for prevention of postendoscopic retrograde cholangiopancreatography pancreatitis

Low dose flurbiprofen for prevention of postendoscopic retrograde cholangiopancreatography pancreatitis - Low dose flurbiprofen for prevention of post endoscopic retrograde cholangiopancreatography pancreatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011322
Enrollment
100
Registered
2013-08-01
Start date
2013-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

all desease that is needed ERCP

Interventions

Patients who were scheduled to undergo ERCP were receive 50 mg of flurbiprofen infusion. The dose of flurbiprofen was reduced to 25 mg in patients weighing&lt
50 kg A medicine is not prescribed for the patient.

Sponsors

YOKOHAMA CITY UNIVERSITY HOSPITAL
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)older than 20years old 2)the patient performed ERCP 3) The patient who understands the details of this research and by whom the consent of research participation is got from himself/herself with a document

Exclusion criteria

Exclusion criteria: 1) acute or active pancreatitis 2)metalicstent was inserted across the papilla 3)history of endoscopic sphincterotomy 4) peptic ulcer diseases 5) aspirin-induced asthma 6) NSAIDs during the preceding 1 week 7) hypersensitivity to NSAIDs 8) pregnant or breast-feeding 9) severe renal dysfunction, 10) the patient whom the doctor in attendance judged to be unsuitable

Design outcomes

Primary

MeasureTime frame
Does pancreatitis happened post ERCP or not

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026