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Thrombin Generation Numerical Models Validation in Haemophilic Case

12 de agosto de 2015 actualizado por: Centre Hospitalier Universitaire de Saint Etienne
Personalized therapy in haemophilia has not been reached yet. Treatment is substitutive and its doses are only based on the levels of deficient factor VIII (for haemophilia A) or IX (for haemophilia B). The bleeding severity is not only related to the factor deficiency but also to levels of other coagulation factors (e.g. factor X, II, AT or TFPI). It's necessary to take them into account in order to individualize treatments; and Thrombin Generation Assay (TGA) with the CAT method (Calibrated Automated Thrombography) is a good way because it measures the result of the coagulation cascade. TGA on Platelet Rich Plasma (PRP) is even closer to physiological conditions than on Platelet Poor Plasma (PPP) because platelet influence is represented. It has already been shown (at least in PPP) that the bleeding tendency in haemophilic patients is usually well correlated to TG. Some TG parameters are used to characterize the individual coagulation phenotype, the most important being the Endogenous Thrombin Potential (ETP) and the Lag Time (LT). A hemorrhagic profile usually provides a longer lag time and / or a lower ETP. However, only few studies tried to determine the influence of each coagulation factor and inhibitor on TG. They were done on Platelet Poor Plasma (PPP) or on lyophilized plasma. So the relation between coagulation factors and the different TG parameters remains to be determined, especially in the haemophilic case. It is possible, experimentally, to find the optimal dose of the factor to be added by measuring TG in samples with different factor VIII or IX concentrations, but this method would be time consuming and expensive, especially because it should be done for each haemophilic patient. A better way consists in using TG numerical models. For a set of initial factor levels they simulate the TG and its associated parameters. It is now essential to validate the existing models, especially in haemophilic cases, in order to see whether they are reliable and can be used in clinical practice afterwards.The objective of this study is to validate thrombin generation numerical models which could predict the factor VIII or IX activity correction to reach a thrombin generation sufficient to avoid bleeding. A comparison between the TG observed in haemophilic patients and the TG predicted by the models is needed to validate the models. In order to define a 'safe' TG i.e. sufficient to avoid bleeding, normal ranges of TG parameters have to be measured.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Tipo de estudio

De observación

Inscripción (Actual)

40

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Saint-Etienne, Francia, 42055
        • CHU Saint-Etienne

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 45 años (Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Masculino

Método de muestreo

Muestra no probabilística

Población de estudio

volunteers witch work in CHU Saint-Etienne

Descripción

Inclusion Criteria:

  • Signed consent form
  • Age between 18 and 45 years old
  • Male
  • no smoker

Exclusion Criteria:

  • other clinical research protocol participation during the 3 months before inclusion
  • Personal or familial history of hemorrhagic disease (parents, brothers and sisters
  • Personal history of thrombosis (arterial or venous)
  • Familial history of thrombosis before 45 years old (parents, brothers and sisters)
  • Drug treatments of aspirin or anti-inflammatory type during the week before sampling
  • Surgery the month before sampling
  • Chronic pathology responsible for inflammatory syndrome
  • Infectious episode in course

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Volunteers
Blood sampling : 1 blood punction of 36.5 ml for each volunteer
Samplings will be taken on 4 citrated S-monovette tubes, 3 citrated tubes and 1 EDTA tube, namely 36.5 ml for each volunteer

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Endogenous Thrombin Potential (ETP) predicted by numerical models
Periodo de tiempo: up to 12 monthes
ETP (i.e. the aera under the thrombin generation curve, nM.min) measured in haemophilic patients is compared to ETP predicted by numerical models.
up to 12 monthes
Lag Time of the thrombin generation curve predicted by numerical models
Periodo de tiempo: up to 12 monthes
Lag time (min) measured in haemophilic patients is compared to the lag time predicted by numerical models
up to 12 monthes
Peak value of the thrombin generation curve predicted by numerical models
Periodo de tiempo: up to 12 monthes
Peak value (nmol thrombin) measured in haemophilic patients is compared to the peak value predicted by numerical models
up to 12 monthes
Time to peak (TTP) of the thrombin generation curve predicted by numerical models
Periodo de tiempo: up to 12 monthes
TTP (min) measured in haemophilic patients is compared to TTP predicted by numerical models
up to 12 monthes
Velocity Index (V) of the thrombin generation curve predicted by numerical models
Periodo de tiempo: up to 12 monthes
Velocity Index measured in haemophilic patients is compared to TTP predicted by numerical models
up to 12 monthes

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Endogenous Thrombin Potential (ETP) for volunteers
Periodo de tiempo: day 1
ETP (i.e. the aera under the thrombin generation curve, nM.min) is measured by Thromboplastin Generation Tests (TGTs)
day 1
Lag Time of the thrombin generation curve for volunteers
Periodo de tiempo: day 1
Lag time (min) of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
day 1
Peak value of the thrombin generation curve for volunteers
Periodo de tiempo: day 1
Peak value of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
day 1
Time to peak (TTP) of the thrombin generation curve for volunteers
Periodo de tiempo: day 1
TTP of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
day 1
Velocity Index (V) of the thrombin generation curve for volunteers
Periodo de tiempo: day 1
Velocity Index (V) of the thrombin generation curves measured by Thromboplastin Generation Tests (TGTs)
day 1

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Brigitte TARDY-PONCET, MD, CHU Saint-Etienne

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de marzo de 2015

Finalización primaria (Actual)

1 de julio de 2015

Finalización del estudio (Actual)

1 de julio de 2015

Fechas de registro del estudio

Enviado por primera vez

18 de noviembre de 2014

Primero enviado que cumplió con los criterios de control de calidad

21 de noviembre de 2014

Publicado por primera vez (Estimar)

25 de noviembre de 2014

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

13 de agosto de 2015

Última actualización enviada que cumplió con los criterios de control de calidad

12 de agosto de 2015

Última verificación

1 de agosto de 2015

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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