Tailored Hydration for the Prevention of Post-ERCP Pancreatitis
Cholangiopancreatography, Endoscopic Retrograde, Pancreatitis
About this trial
This is an interventional prevention trial for Cholangiopancreatography, Endoscopic Retrograde focused on measuring Endoscopic retrograde pancreatocholangiography, Pancreatitis, Lactate ringer's solution, Tailored therapy
Eligibility Criteria
Inclusion Criteria:
- All patients older than 20 years undergoing ERCP for the 1st time will be recruited
Exclusion Criteria:
- Age below 20 or above 80 years
- Underlying severe psychiatric illness
- Cardiac insufficiency (>New York Heart Association Class II heart failure)
- Renal insufficiency (eGFR <30mililiter/min/1.73m2)
- Respiratory insufficiency (defined as oxygen saturation < 90%)
- Poorly controlled blood sugar
- Ongoing hypotension including those with sepsis
- Ongoing acute pancreatitis
- Underlying disease of chronic pancreatitis
- Clinical signs of hypervolemia
- Hyponatremia (Na+ levels < 130 milliequivalent (mEq)/L))
- Hypernatremia (Na+ levels > 150mEq/L)
- Hyperkalemia (5.1 mEq/dL)
- Metabolic alkalosis
- Past history of endoscopic sphincterectomy or endoscopic papillary balloon dilatation
Sites / Locations
- Chonnam National University Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Tailored standard hydration
Tailored aggressive hydration
Patients will be randomly allocated to tailored standard hydration arm. Patients will receive hydration with lactated Ringer's solution with rate of 1.5 milliliter(mL)/kg/hr during and after ERCP. Hydration and feeding will be tailored by each patient's symptoms and serum amylase levels.
Patients will be randomly allocated to tailored aggressive hydration arm. Patients will receive hydration with lactated Ringer's solution with rate of 3.0 milliliter(mL)/kg/hr during and after ERCP and bolus injection of 20mL/kg over 1 hour after ERCP. Hydration and feeding will be tailored by each patient's symptoms and serum amylase levels.