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NCT06312488: POCEFIS

Point of Care Evaluation of Fibrinolysis in Sepsis

Completed NA Last updated 8 April 2026
What this trial tests

NA trial testing Clot Pro in Fibrinolytic Defect in 100 participants. Completed in 30 November 2025.

Timeline
22 January 2024
Primary endpoint
31 March 2025
30 November 2025

Quick facts

Lead sponsorPoliclinico Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment100
Start date22 January 2024
Primary completion31 March 2025
Estimated completion30 November 2025
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Policlinico Hospital

Who can join

18 and older, any sex, with Fibrinolytic Defect or Sepsis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Abstracts of the ICARE 2025 79th SIAARTI National Congress.
    · 2025 · PMID 41111139 · DOI 10.1186/s44158-025-00273-8

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Other Policlinico Hospital trials

Trials by the same sponsor.

Verify against primary sources

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/NCT06312488.

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