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NCT06680180: FORTITUDE

Fibrinolysis Resistance in Infection and Trauma

Recruiting now Last updated 8 November 2024
What this trial tests

trial testing Viscoelastometric assessment of fibrinolysis in Sepsis and Septic Shock in 150 participants. Currently enrolling.

Timeline
1 June 2024
Primary endpoint
31 December 2025
1 June 2026

Quick facts

Lead sponsorAnders Aneman
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment150
Start date1 June 2024
Primary completion31 December 2025
Estimated completion1 June 2026
Sites4 locations across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Anders Aneman

Who can join

18 and older, any sex, with Sepsis and Septic Shock or Trauma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Blood coagulation disorders are often seen in critically ill patients e.g. with severe infection or following extensive injury, that can lead to life threatening events as a result of excessive blood clot formation leading to organ failure. This study aims to use Viscoelastic Testing (VET) technology to detect patients at risk of excessive blood blot formation at the bedside, test new blood coagulation drugs, and guide life-saving use of blood modifying treatments.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Sepsis and Septic Shock

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06680180.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing