Efficacy of Administration of Somatostatin in the Prevention of Post-endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis (crepsmt1)
Acute Pancreatitis
About this trial
This is an interventional prevention trial for Acute Pancreatitis focused on measuring acute pancreatits
Eligibility Criteria
Inclusion criteria:
- Patients undergoing therapeutic endoscopic retrograde cholangiopancreatography (ERCP).
Exclusion Criteria:
- Pregnancy or history of allergy to somatostatin.
- Acute myocardial infarction within 3 months of the procedure.
- Acute pancreatitis in patients undergoing early ERCP in the acute phase of the disease.
- Previous sphincterotomy.
- Chronic pancreatitis.
Sites / Locations
- Endoscopy Unit Hospital de la Santa Creu i Sant PauRecruiting
- Hospital de la Santa Creu i Sant PauRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
somatostatin, intravenous bolus
Placebo, intravenous bolus
A double- blind study designed to evaluate if the treatment with somatostatin in intravenous bolus before starting the ERCP procedure followed by a continuous infusion for 4 hours after endoscopic proof could prevent acute post-ERCP pancreatitis. Patients submitted to ERCP will be randomized in two groups of treatment, one will receive somatostatin and another placebo.
A double- blind study designed to evaluate if the treatment with somatostatin in intravenous bolus before starting the ERCP procedure followed by a continuous infusion for 4 hours after endoscopic proof could prevent acute post-ERCP pancreatitis. Patients submitted to ERCP will be randomized in two groups of treatment, one will receive somatostatin and another placebo.