MedTrace Logo

F-Point Validation Study

NCT03623061 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2018-08-09

No results posted yet for this study

Summary

The F-Point investigation is an open label, single centre prospective observational study in 3 cohorts of patients, one with low fibrinogen concentration, one with normal fibrinogen concentration, and one with high fibrinogen concentration To show statistical agreement between the fibrinogen level as recorded by the standard lab Clauss fibrinogen, and the fibrinogen level as recorded by the novel F-Point device.

Conditions

  • Low Fibrinogen

Interventions

DIAGNOSTIC_TEST

F-Point

F-Point (point of care in vitro diagnostic device for measuring plasma fibrinogen concentration)

Sponsors & Collaborators

  • Dublin City University

    collaborator OTHER

  • Enterprise Ireland

    collaborator OTHER_GOV

  • Royal College of Surgeons, Ireland

    lead OTHER

Principal Investigators

  • Patrick Thornton · Rotunda Hospital

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-14
Primary Completion
2018-10-30
Completion
2018-10-30

Countries

  • Ireland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03623061 on ClinicalTrials.gov