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Point of Care Evaluation of Fibrinolysis in Sepsis — POCEFIS  

Sepsis Clinical Trial

Official title:
Point of Care Evaluation of Fibrinolysis in Sepsis

Clinical Trial Summary

Impaired fibrinolysis in septic patients is associated with worse outcome. The present study investigates fibrinolysis shutdown in septic patients, defined as prolonged ClotPro® TPA lysis time at 30 minutes. The TPA lysis time reference range is established in a cohort of healthy volunteers.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06312488
Study type Interventional
Source Policlinico Hospital
Contact
Status Recruiting
Phase N/A
Start date January 22, 2024
Completion date August 31, 2025
View Details
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