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Comparative Evaluation of the Performance of Different Thromboplastin Reagents on Prothrombin Time and Factorial Assays in Situations of Isolated Extrinsic Pathway Factor Deficiency or Liver Damage.

U

University Hospital, Strasbourg, France

Status

Enrolling

Conditions

Hemorrhagic Disorders
Extrinsic Pathway Factor Deficiency
Hepatocellular Insufficiency With Coagulopathy

Treatments

Biological: Prothrombin

Study type

Observational

Funder types

Other

Identifiers

NCT06705829
IV-0196

Details and patient eligibility

About

Primary purpose :

Compare the sensitivity of several thromboplastin reagents of various origins to prothrombin time and factor II, V, VII and X assays in two different populations of patients :

  • Patients with an isolated extrinsic pathway deficiency (acquired or congenital) of factor II or V or VII or X.
  • Patients with an hepatocellular insufficiency generally associated with coagulopathy (with an intensity proportional to the degree of hepatic impairment).

Results of this work should improve knowledge of sensitivity of the screening test represented by the prothrombin time, depending on the origin of thromboplastin reagent used, in relation with coagulopathies mentioned above, as well as the performance of factors II, V, VII, X assays. This work would help to choice of the most suitable reagent for the needs of each hemostasis laboratory/center.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

  • Plasma samples from patients addressed to the laboratory of the Strasbourg University Hospital (Strasbourg France) collected and anonymized after completion of the routine testing.
  • Patient with an isolated or combined extrinsic pathway factor deficiency (factor II, V, VII, X).

Exclusion criteria :

  • Patient treated with an oral anticoagulant treatment.
  • Patient treated with a parenteral anticoagulant treatment (apart from therapeutic dosages of unfractionated heparin and low molecular weight heparin).

Trial design

100 participants in 1 patient group

Hepatocellular insufficiency with coagulopathy
Description:
Patients with an hepatocellular insufficiency generally associated with coagulopathy (with an intensity proportional to the degree of hepatic impairment).
Treatment:
Biological: Prothrombin

Trial contacts and locations

1

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Central trial contact

Jordan Laurent WIMMER

Data sourced from clinicaltrials.gov

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