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Efficacy of suppository naproxen in prevention of pancreatitis

Phase 2
Conditions
acute pancreatitis.
other acute pancreatitis
Registration Number
IRCT201105301155N14
Lead Sponsor
Behvazan Company
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
324
Inclusion Criteria

All patients over 18 years who were referred to hospital for ERCP; disorders in liver function tests; had extrahepatic cholestasis.
Exclusion criteria: Acute pancreatitis in the last two weeks; history of chronic pancreatitis; a history of previous sphincterotomy; NSAID use in a week; contraindication for NSAID use such as renal failure and having allergy to the drug; peptic ulcer with recent GI bleeding; not consent to participate in this plan.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pancreatitis. Timepoint: 24 hours after ERCP. Method of measurement: Amylase serum, Patient's symptoms(nausea, vomiting and abdominal pain).
Secondary Outcome Measures
NameTimeMethod
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