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Thrombin Generation Numerical Models Validation in Haemophilic Case
12 augustus 2015 bijgewerkt door: 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.
Studie Overzicht
Studietype
Observationeel
Inschrijving (Werkelijk)
40
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Saint-Etienne, Frankrijk, 42055
- Chu Saint-Etienne
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 45 jaar (Volwassen)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Mannelijk
Bemonsteringsmethode
Niet-waarschijnlijkheidssteekproef
Studie Bevolking
volunteers witch work in CHU Saint-Etienne
Beschrijving
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
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
|---|---|
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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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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Endogenous Thrombin Potential (ETP) predicted by numerical models
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: up to 12 monthes
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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
Tijdsspanne: 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
Tijdsspanne: 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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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Endogenous Thrombin Potential (ETP) for volunteers
Tijdsspanne: 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
Tijdsspanne: day 1
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Lag time (min) of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
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day 1
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Peak value of the thrombin generation curve for volunteers
Tijdsspanne: day 1
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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
Tijdsspanne: day 1
|
TTP of the thrombin generation curve is measured by Thromboplastin Generation Tests (TGTs)
|
day 1
|
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Velocity Index (V) of the thrombin generation curve for volunteers
Tijdsspanne: day 1
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Velocity Index (V) of the thrombin generation curves measured by Thromboplastin Generation Tests (TGTs)
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day 1
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Onderzoekers
- Hoofdonderzoeker: Brigitte TARDY-PONCET, MD, Chu Saint-Etienne
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 maart 2015
Primaire voltooiing (Werkelijk)
1 juli 2015
Studie voltooiing (Werkelijk)
1 juli 2015
Studieregistratiedata
Eerst ingediend
18 november 2014
Eerst ingediend dat voldeed aan de QC-criteria
21 november 2014
Eerst geplaatst (Schatting)
25 november 2014
Updates van studierecords
Laatste update geplaatst (Schatting)
13 augustus 2015
Laatste update ingediend die voldeed aan QC-criteria
12 augustus 2015
Laatst geverifieerd
1 augustus 2015
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 1408185
- 2014-A01734-43 (Andere identificatie: ANSM - FRANCE)
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .