Pancreatitis Clinical Trial
Official title:
Randomized Trial of Standard vs. Enhanced Hydration in Patients With a Diagnosis of Acute Pancreatitis Within the First Hour of the Diagnosis
The aim of this study is to establish the influence of early administration of a bolus of intravascular fluid in patients with a diagnosis of acute pancreatitis on the course and outcome of disease.
Status | Recruiting |
Enrollment | 903 |
Est. completion date | September 2018 |
Est. primary completion date | March 2018 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: All patients with diagnosis of acute pancreatitis. Exclusion Criteria: 1. Refusal to sign informed consent 2. Age less than 18 years 3. Pregnancy 4. Patients with physical signs of heart failure, 5. Previously known congestive heart failure ( NYHA III - IV ) 6. Severe kidney disease more than one month before the diagnosis of acute pancreatitis (defined as severe reduction in eGFR less than 30 ml/min/1.73 m2) . Patients who develop acute renal failure as a result of acute pancreatitis will be involved in research . |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Croatia | UHRijeka | Rijeka |
Lead Sponsor | Collaborator |
---|---|
University Hospital Rijeka |
Croatia,
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* Note: There are 33 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction of mortality | Number of participants with fatal outcome during hospitalisation | Until hospital discharge or maximum of 1 month | No |
Primary | Development of severe pancreatitis | Number of participants with severe pancreatitis during hospitalisation (according to revised Atlanta criteria) | Until hospital discharge or maximum of 1 month | No |
Secondary | Development of peripancreatic collection | Number of participants with development of peripancreatic collection during hospitalisation | Until hospital discharge or maximum of 1 month | No |
Secondary | Development of pancreatic collection infection | Number of participants with development of pancreatic collection infection during hospitalisation | Until hospital discharge or maximum of 1 month | No |
Secondary | Development of systemic inflammatory response syndrome (SIRS) | Number of participants with development of systemic inflammatory response syndrome (SIRS) | Until hospital discharge or maximum of 1 month | No |
Secondary | Development of metabolic acidosis | Number of participants with development of metabolic acidosis | Until hospital discharge or maximum of 1 month | No |
Secondary | Development of acute respiratory distress syndrome (ARDS ) defined according to the current Berlin definition | Number of participants with development of acute respiratory distress syndrome (ARDS ) defined according to the current Berlin definition | Until hospital discharge or maximum of 1 month | No |
Secondary | Adverse events | All events during the treatment of patients who may or may not be associated with acute pancreatitis and / or replacement of fluids | Until hospital discharge or maximum of 1 month | No |
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