Fluid Resuscitation With HES 200/0.5 10% in Severe Burn Injury

Status Completed

Clinical Trial Summary

HES 200/0.5 10% is equal to ringers lactat solution.

Clinical Trial Description

30 Patients were enrolled to the study, either to the hyperoncotic HES 200/0.5 (10%) group or to the crystalloids only group. After a treatment protocol of 72 hours we collected data about complications like pulmonary failure and abdominal compartment syndrome. Furthermore, we addressed the question of incidence of mortality and renal failure. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01120730
Study type	Interventional
Source	University of Zurich
Contact
Status	Completed
Phase	Phase 3
Start date	April 1997
Completion date	March 2009

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