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Compare intense hydration and fluid standard therapy before and after of ERCP in the prevention of post ERCP pancreatitis

Not Applicable
Conditions
Other Acute Pancreatitis
k85.8
Acute Pancreatitis.
Registration Number
IRCT20191226045897N1
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
160
Inclusion Criteria

All patients over 18 years who were referred to hospital for ERCP.
Patients disorders in liver function tests or had extrahepatic cholestasis.

Exclusion Criteria

History of PEP and Pancreatitis with Other Pancreatic Risk Factors and Diseases
Heart Failure
IBD
NSAID Allergy
Coagulation Disorders
Chronic renal failure
Current hypotension (eg septic shock)
Severe liver failure
Respiratory failure
Pregnancy
Hyponatremia or Hypnothermia
Edema or ascites
Using high-risk outside the stone during the ERCP procedure

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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