Balanced Crystalloid Solutions for Acute Pancreatitis

Status Recruiting

Clinical Trial Summary

Patients diagnosed with acute pancreatitis regardless of etiology, severity of disease, and prior attacks will be randomized in two groups. The intervention group will receive a balanced crystalloid (Plasmalyte) at a rate of 10 ml/kg during the first 60 min and then continued at 3 ml/kg/h for the next 72 hours. The control group will receive normal saline at the same rate.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04688645
Study type	Interventional
Source	University Hospital Rijeka
Contact	Goran Poropat, MD, PhD
Phone	0038551658191
Email	gporopat8@gmail.com
Status	Recruiting
Phase	Phase 4
Start date	May 1, 2020
Completion date	February 1, 2023

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