None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? In cases who visit the emergency room for symptoms of acute pancreatitis and contact this clinical researcher within 6 hours ? Mild or moderate acute pancreatitis ? Patients who agree to participate in this study and complete the patient consent form
Exclusion criteria
Exclusion criteria: ? Severe acute pancreatitis ? New York Heart Association Class > II heart failure, ? Pulmonary edema, ? Renal failure (Cr > 1.9 mg/dL) ? Abnormal liver function (albumin < 3 mg/dL, or liver cirrhosis diagnosis) ? Clinical signs of hypervolemia: pulmonary congestion, peripheral edema, ascites ? Under the age of 18 ? Pregnancy ? Patient who does not agree to clinical trials
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the prevalence of SIRS(Systemic inflammatory response syndrome) after 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| CRP after 24 hours, local complications, organ failure, progression to moderate or severe acute pancreatitis, intensive care unit admission, invasive treatment rate, length of hospitalization, mortality, pH and bicarbonate after 24 hours. | — |
Countries
Korea, Republic of
Contacts
The Catholic University of Korea, Uijeongbu St. Mary’s Hospital