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Shock Index To DEtect Low Plasma Fibrinogen In Trauma (SIDE) — SIDE  

Trauma, Multiple Clinical Trial

Official title:
Shock Index To DEtect Low Plasma Fibrinogen In Trauma (SIDE)

Clinical Trial Summary

Shock-index is potentially an easy tool to estimate the risk of hypofibrinogenemia without the need to perform other potentially time consuming investigations.

Clinical Trial Description

Hypofibrinogenemia is common in severe trauma and below the threshold of 2.3 g/l is associated with increased mortality. Although guidelines for management of the trauma induced coagulopathy does not recommend any specific timing of fibrinogen substitution, several papers suggest that early substitution might be associated with improved outcome. Laboratory measurement of plasma fibrinogen level, thromboelastometry and/or its estimation based on base excess, hemoglobin level, Injury Severity Score or combinations require diagnostic procedures that are associated with with a certain time delay and prolongs the time to fibrinogen substitution. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02619539
Study type Observational [Patient Registry]
Source Masaryk Hospital Krajská zdravotní a.s.
Contact
Status Completed
Phase N/A
Start date January 2016
Completion date February 28, 2017
View Details
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