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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


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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