pancreatitis. Other acute pancreatitis
Conditions
Interventions
Group1: Adminstration of single dose of 100 mg rectal indomethacine just before doing Endoscopic cholangiopancreatography Group2: Administration of single dose of 100 mg rectal Indomethacine plus 500
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients undergoing ERCP in Taleghani hospital by taking written consent
Exclusion criteria
Exclusion criteria: Patients history of hypersensitivity against each of indomethacin or vitamin C Active peptic ulcer diseases Renal impairment (GFR < 10 ml/min)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pancreatitis. Timepoint: 10 days after doing ERCP. Method of measurement: clinical evaluation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Gastrointestinal bleeding. Timepoint: 10 days after doing ERCP. Method of measurement: Clinical observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Abbasinazari
Shahid Beheshti University of Medical Sciences
Outcome results
None listed