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- Essai clinique NCT02300519
Thrombin Generation Numerical Models Validation in Haemophilic Case
12 août 2015 mis à jour par: 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.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Type d'étude
Observationnel
Inscription (Réel)
40
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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-
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Saint-Etienne, France, 42055
- Chu Saint-Etienne
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans à 45 ans (Adulte)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Homme
Méthode d'échantillonnage
Échantillon non probabiliste
Population étudiée
volunteers witch work in CHU Saint-Etienne
La description
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 d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
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Volunteers
Blood sampling : 1 blood punction of 36.5 ml for each volunteer
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Samplings will be taken on 4 citrated S-monovette tubes, 3 citrated tubes and 1 EDTA tube, namely 36.5 ml for each volunteer
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Endogenous Thrombin Potential (ETP) predicted by numerical models
Délai: up to 12 monthes
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ETP (i.e. the aera under the thrombin generation curve, nM.min)
measured in haemophilic patients is compared to ETP predicted by numerical models.
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up to 12 monthes
|
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Lag Time of the thrombin generation curve predicted by numerical models
Délai: up to 12 monthes
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Lag time (min) measured in haemophilic patients is compared to the lag time predicted by numerical models
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up to 12 monthes
|
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Peak value of the thrombin generation curve predicted by numerical models
Délai: up to 12 monthes
|
Peak value (nmol thrombin) measured in haemophilic patients is compared to the peak value predicted by numerical models
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up to 12 monthes
|
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Time to peak (TTP) of the thrombin generation curve predicted by numerical models
Délai: up to 12 monthes
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TTP (min) measured in haemophilic patients is compared to TTP predicted by numerical models
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up to 12 monthes
|
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Velocity Index (V) of the thrombin generation curve predicted by numerical models
Délai: up to 12 monthes
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Velocity Index measured in haemophilic patients is compared to TTP predicted by numerical models
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up to 12 monthes
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Endogenous Thrombin Potential (ETP) for volunteers
Délai: day 1
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ETP (i.e. the aera under the thrombin generation curve, nM.min) is measured by Thromboplastin Generation Tests (TGTs)
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day 1
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Lag Time of the thrombin generation curve for volunteers
Délai: day 1
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Lag time (min) of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
|
day 1
|
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Peak value of the thrombin generation curve for volunteers
Délai: day 1
|
Peak value of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
|
day 1
|
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Time to peak (TTP) of the thrombin generation curve for volunteers
Délai: 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
Délai: day 1
|
Velocity Index (V) of the thrombin generation curves measured by Thromboplastin Generation Tests (TGTs)
|
day 1
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Les enquêteurs
- Chercheur principal: Brigitte TARDY-PONCET, MD, Chu Saint-Etienne
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 mars 2015
Achèvement primaire (Réel)
1 juillet 2015
Achèvement de l'étude (Réel)
1 juillet 2015
Dates d'inscription aux études
Première soumission
18 novembre 2014
Première soumission répondant aux critères de contrôle qualité
21 novembre 2014
Première publication (Estimation)
25 novembre 2014
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
13 août 2015
Dernière mise à jour soumise répondant aux critères de contrôle qualité
12 août 2015
Dernière vérification
1 août 2015
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 1408185
- 2014-A01734-43 (Autre identifiant: ANSM - FRANCE)
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .