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Evaluation & safety of lactated ringer’s solution on prevention of acute pancreatitis

Not Applicable
Recruiting
Conditions
Acute pancreatitis.
Acute pancreatitis
Registration Number
IRCT20171009036664N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
164
Inclusion Criteria

Indication for endoscopic retrograde cholangiopancreaticography (ERCP);
Consent of enrollment in the study

Exclusion Criteria

Acute cholangitis;
Sepsis;
Pregnancy;
Age above 70 years;
Chronic pancreatitis;
Acute pancreatitis due to billiary stone;
evidence of fluid overload;
Peripheral edema;
Pulmonary edema;
Electrolyte disturbance for example Na over 150 or below 130;
Cirrhosis
Renal failure
History of endoscopic retrograde cholangiopancreaticography performation with sphinctrotomy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post endoscopicretrograde cholangiopancreatography pancreatitis. Timepoint: 6, 12 and 24 hours after endoscopicretrograde cholangiopancreatography procedure. Method of measurement: Clinical examination (abdominal pain) & laboratory testing(amylase, and/or lipase levels to =3 times the upper limit of normal).
Secondary Outcome Measures
NameTimeMethod
Complications of ERCP. Timepoint: 6, 12 and 24 hours after endoscopicretrograde cholangiopancreatography procedure. Method of measurement: Clinical examination.
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