Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Thrombin Generation Numerical Models Validation in Haemophilic Case

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.

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Studietype

Observasjonsmessig

Registrering (Faktiske)

40

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Saint-Etienne, Frankrike, 42055
        • Chu Saint-Etienne

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 45 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Mann

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
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

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Endogenous Thrombin Potential (ETP) predicted by numerical models
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: up to 12 monthes
Velocity Index measured in haemophilic patients is compared to TTP predicted by numerical models
up to 12 monthes

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Endogenous Thrombin Potential (ETP) for volunteers
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: day 1
Velocity Index (V) of the thrombin generation curves measured by Thromboplastin Generation Tests (TGTs)
day 1

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Brigitte TARDY-PONCET, MD, Chu Saint-Etienne

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. mars 2015

Primær fullføring (Faktiske)

1. juli 2015

Studiet fullført (Faktiske)

1. juli 2015

Datoer for studieregistrering

Først innsendt

18. november 2014

Først innsendt som oppfylte QC-kriteriene

21. november 2014

Først lagt ut (Anslag)

25. november 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

13. august 2015

Siste oppdatering sendt inn som oppfylte QC-kriteriene

12. august 2015

Sist bekreftet

1. august 2015

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere