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Fluid Resuscitation in Acute Pancreatitis

Primary Purpose

Pancreatitis

Status
Unknown status
Phase
Phase 2
Locations
Croatia
Study Type
Interventional
Intervention
Ringer lactate
Sponsored by
University Hospital Rijeka
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatitis focused on measuring Acute pancreatitis, Fluid resuscitation, Crystalloids

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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 .

Sites / Locations

  • UHRijekaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Ringer lactate 20 mL/kg

Ringer lactate 40 ml/kg

Arm Description

This group of subjects will receive a bolus of 20 ml / kg of Ringer's solution for infusion within first hour of the diagnosis

This group of subjects will receive a bolus of 40 ml / kg of Ringer's solution for infusion within first hour of the diagnosis

Outcomes

Primary Outcome Measures

Reduction of mortality
Number of participants with fatal outcome during hospitalisation
Development of severe pancreatitis
Number of participants with severe pancreatitis during hospitalisation (according to revised Atlanta criteria)

Secondary Outcome Measures

Development of peripancreatic collection
Number of participants with development of peripancreatic collection during hospitalisation
Development of pancreatic collection infection
Number of participants with development of pancreatic collection infection during hospitalisation
Development of systemic inflammatory response syndrome (SIRS)
Number of participants with development of systemic inflammatory response syndrome (SIRS)
Development of metabolic acidosis
Number of participants with development of metabolic acidosis
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
Adverse events
All events during the treatment of patients who may or may not be associated with acute pancreatitis and / or replacement of fluids

Full Information

First Posted
March 10, 2016
Last Updated
March 10, 2016
Sponsor
University Hospital Rijeka
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1. Study Identification

Unique Protocol Identification Number
NCT02709044
Brief Title
Fluid Resuscitation in Acute Pancreatitis
Official Title
Randomized Trial of Standard vs. Enhanced Hydration in Patients With a Diagnosis of Acute Pancreatitis Within the First Hour of the Diagnosis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
March 2018 (Anticipated)
Study Completion Date
September 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Rijeka

4. Oversight

5. Study Description

Brief Summary
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.
Detailed Description
This is a prospective, randomized, controlled clinical trial of standard versus enhanced hydration in patients diagnosed with acute pancreatitis within the first hour of diagnosis. Patients admitted in the Emergency Department with the clinical suspicion of acute pancreatitis will be processed through the history, physical examination and laboratory findings. The diagnosis of acute pancreatitis is established by the presence of 2 of the 3 following criteria: typical abdominal pain, serum amylase and / or lipase greater than three times the upper limit of normal, and characteristic findings from abdominal imaging. Patients will be informed about the study protocol and the possible risks and adverse events, after which they will be asked to accept participation in the study. Acceptance of participation will be confirmed by signed informed consent. After acceptance patients will be randomized by computer-generated sequences of random numbers in the two groups Group one (1) will receive a bolus of fluid 20 ml / kg of Ringer's solution for infusion within one hour of the diagnosis and the group two (2) will receive a bolus of fluid 40 ml / kg of Ringer's solution for infusion within one hour of the diagnosis. All patients who have the diagnosis of acute pancreatitis, but did not agree to participate in research or have some other exclusion criteria will be treated according to the standards of good clinical practice and the recommendations of the current clinical guidelines for the treatment of acute pancreatitis. Exclusion criteria beside refusal to sign informed consent are: age less than 18 years, pregnancy, patients with physical signs of heart failure, previously known congestive heart failure (NYHA III - IV) and 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 . Given the importance of early hydration in patients with acute pancreatitis and the lack of clearly defined dose of administered fluid in the current literature, aim of this study was to determine the influence of the size of the dose bolus of intravascular fluid after the diagnosis of acute pancreatitis in the further course and outcome of disease. The study will be conducted in the Emergency Department, Clinical Hospital Centre, Rijeka.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatitis
Keywords
Acute pancreatitis, Fluid resuscitation, Crystalloids

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
903 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ringer lactate 20 mL/kg
Arm Type
Experimental
Arm Description
This group of subjects will receive a bolus of 20 ml / kg of Ringer's solution for infusion within first hour of the diagnosis
Arm Title
Ringer lactate 40 ml/kg
Arm Type
Experimental
Arm Description
This group of subjects will receive a bolus of 40 ml / kg of Ringer's solution for infusion within first hour of the diagnosis
Intervention Type
Drug
Intervention Name(s)
Ringer lactate
Primary Outcome Measure Information:
Title
Reduction of mortality
Description
Number of participants with fatal outcome during hospitalisation
Time Frame
Until hospital discharge or maximum of 1 month
Title
Development of severe pancreatitis
Description
Number of participants with severe pancreatitis during hospitalisation (according to revised Atlanta criteria)
Time Frame
Until hospital discharge or maximum of 1 month
Secondary Outcome Measure Information:
Title
Development of peripancreatic collection
Description
Number of participants with development of peripancreatic collection during hospitalisation
Time Frame
Until hospital discharge or maximum of 1 month
Title
Development of pancreatic collection infection
Description
Number of participants with development of pancreatic collection infection during hospitalisation
Time Frame
Until hospital discharge or maximum of 1 month
Title
Development of systemic inflammatory response syndrome (SIRS)
Description
Number of participants with development of systemic inflammatory response syndrome (SIRS)
Time Frame
Until hospital discharge or maximum of 1 month
Title
Development of metabolic acidosis
Description
Number of participants with development of metabolic acidosis
Time Frame
Until hospital discharge or maximum of 1 month
Title
Development of acute respiratory distress syndrome (ARDS ) defined according to the current Berlin definition
Description
Number of participants with development of acute respiratory distress syndrome (ARDS ) defined according to the current Berlin definition
Time Frame
Until hospital discharge or maximum of 1 month
Title
Adverse events
Description
All events during the treatment of patients who may or may not be associated with acute pancreatitis and / or replacement of fluids
Time Frame
Until hospital discharge or maximum of 1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients with diagnosis of acute pancreatitis. Exclusion Criteria: Refusal to sign informed consent Age less than 18 years Pregnancy Patients with physical signs of heart failure, Previously known congestive heart failure ( NYHA III - IV ) 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 .
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vanja Giljača, M.D. PhD
Phone
+38551658885
Email
vanja.giljača@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Petra Šverko, M.D.
Phone
+38598247655
Email
petrasverko@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vanja Giljača, M.D. PhD
Organizational Affiliation
University Hospital Rijeka
Official's Role
Study Chair
Facility Information:
Facility Name
UHRijeka
City
Rijeka
ZIP/Postal Code
51000
Country
Croatia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vanja Giljača, M.D. PhD
Phone
+38551658380
Email
vanja.giljaca@gmail.com
First Name & Middle Initial & Last Name & Degree
Petra Šverko, M.D.
Phone
+38551658380
Email
petrasverko@gmail.com

12. IPD Sharing Statement

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Fluid Resuscitation in Acute Pancreatitis

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