- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02300519
Thrombin Generation Numerical Models Validation in Haemophilic Case
12. august 2015 opdateret af: 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.
Studieoversigt
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
40
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Saint-Etienne, Frankrig, 42055
- CHU Saint-Etienne
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 45 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Han
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
volunteers witch work in CHU Saint-Etienne
Beskrivelse
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
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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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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Endogenous Thrombin Potential (ETP) predicted by numerical models
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Endogenous Thrombin Potential (ETP) for volunteers
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Brigitte TARDY-PONCET, MD, CHU Saint-Etienne
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. marts 2015
Primær færdiggørelse (Faktiske)
1. juli 2015
Studieafslutning (Faktiske)
1. juli 2015
Datoer for studieregistrering
Først indsendt
18. november 2014
Først indsendt, der opfyldte QC-kriterier
21. november 2014
Først opslået (Skøn)
25. november 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
13. august 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. august 2015
Sidst verificeret
1. august 2015
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 1408185
- 2014-A01734-43 (Anden identifikator: ANSM - FRANCE)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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