- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07666191
REF-VALUE Study: Establishment of Reference Values for Biomarkers in Healthy Adults (REF-VALUE Stud)
Circulating biomarkers play a central role in translational research and precision medicine, particularly for the diagnosis, prognostic, monitoring of inflammatory or infectious diseases and patient stratification. Advances in analytical technologies enable standardised, sensitive and multiplexed assays, but their application remains limited by the lack of reliable reference values derived from well-characterised healthy populations. Indeed, the available data are often heterogeneous and difficult to transfer between platforms.
In this context, the establishment of institutional reference cohorts appears essential for the correct interpretation of immunological parameters-which could be strongly influenced by demographic and clinical factors-and for defining relevant cut-off values when identifying new biomarkers of interest. This issue is particularly critical in the field of viral respiratory infections, where current diagnostic approaches still have several limitations.
Circulating biomarkers play a central role in translational research and precision medicine, particularly for the diagnosis, prognostic, monitoring of inflammatory or infectious diseases and patient stratification. Advances in analytical technologies enable standardised, sensitive and multiplexed assays, but their application remains limited by the lack of reliable reference values derived from well-characterised healthy populations. Indeed, the available data are often heterogeneous and difficult to transfer between platforms.
In this context, the establishment of institutional reference cohorts appears essential for the correct interpretation of immunological parameters-which could be strongly influenced by demographic and clinical factors-and for defining relevant cut-off values when identifying new biomarkers of interest. This issue is particularly critical in the field of viral respiratory infections, where current diagnostic approaches still have several limitations.
Diagnosis is usually based on PCR tests targeting the DNA or RNA of pathogens, requiring a virus-specific test. In practice, only a few viruses (SARS-CoV-2, RSV, influenza) are tested for as a first-line investigation, whilst many other agents may be involved. As a comprehensive approach is difficult to achieve, viral infections often remain under-reported.
Furthermore, the detection of a virus by PCR may indicate either an active infection or residual traces of a past infection. Although viral load can aid interpretation, it does not always allow for a definitive conclusion, making it difficult to distinguish between ongoing viral replication and the persistence of genetic material. It is therefore necessary to have additional markers associated with active infection.
In this context, analysing the host response represents a promising alternative. Viruses induce, in particular, the production of type I interferons (IFN-I), the measurement of which could point the diagnosis towards a viral origin and reflect ongoing infectious activity. However, the interpretation of these biomarkers requires robust reference standards, taking into account their variability across individuals and contexts.
Several studies illustrate the value of such approaches, such as the REFIPA study (NCT07239830), conducted in subjects over 80 years of age, which aims to characterise the immune response, particularly IFN-I, in the context of immunosenescence. This type of study highlights the need for well-phenotyped healthy ? control populations according to age groups and clinical contexts.
Finally, beyond the creation of reference databases, the development of biobanks appears essential. This would enable the establishment of harmonised and directly usable reference values, thereby facilitating translational, basic and pre-clinical research projects, as well as the identification and validation of new biomarkers.
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Typ studie
Zápis (Odhadovaný)
Fáze
- Nelze použít
Kontakty a umístění
Studijní kontakt
- Jméno: Sophie TROUILLET-ASSANT
- Telefonní číslo: +33 4 72 67 87 80
- E-mail: sophie.trouillet-assant@chu-lyon.fr
Studijní záloha kontaktů
- Jméno: William MOUTON
- Telefonní číslo: +33 4 72 67 87 85
- E-mail: william.mouton@chu-lyon.fr
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
Inclusion Criteria:
- Participants aged between 18 and 65 years (inclusive)
- Participants with no known medical conditions
- Body weight of 50 kg or more
Exclusion Criteria:
Participants with symptoms of an active infection (symptom questionnaire or temperature > 37.5°C).
- Subjects participating in another interventional study with an exclusion period that is still ongoing or that may interfere with this protocol
- Pregnant women, women in labour or breastfeeding women
- Individuals deprived of their liberty by a judicial or administrative decision
- Individuals receiving psychiatric care
- Individuals admitted to a health or social care facility for purposes other than research
- Adults subject to legal protection measures (guardianship, curatorship)
- Individuals not affiliated with a social security scheme or beneficiaries of a similar scheme
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Jiný
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: Healthy volunteers
Healthy, uninfected adults aged 18 to 65 inclusive.
Participants may be recruited through the press and social media, via the staff mailing list of the Hospices Civils de Lyon, or via posters displayed within the hospital aimed at staff, as well as at patients' carers and any other interested individuals.
|
The procedures specifically carried out for the study are as follows:
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
To establish reference values for the nasal and blood type I interferon score in an uninfected adult population aged 18 to 65 years inclusive.
Časové okno: One day
|
The primary endpoint is the measurement of nasal and blood interferon levels in a population of uninfected adults aged 18 to 65 years inclusive.
|
One day
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
To assess the impact of immune parameters on baseline blood and nasal IFN-I scores
Časové okno: One day
|
Correlation between immune parameters assessed by anti-IFN antibody concentration, the abundance of key immune cell subpopulations, lymphocyte function assessed by functional immune testing (such as IGRA), and the baseline blood and nasal interferon score
|
One day
|
|
To assess the impact of demographic and clinical parameters on baseline blood and nasal IFN-I scores
Časové okno: One day
|
Correlation between demographic (age, sex) and clinical parameters, and the baseline blood and nasal interferon score
|
One day
|
|
Compare baseline IFN-I levels between two subgroups of participants initially considered uninfected: those in whom the PCR test routinely performed on the day of the visit detects no infection, and those in whom this PCR test reveals an asymptomatic infe
Časové okno: One day
|
Mean (or median) variation in IFN-I between the two groups, with estimation of the effect size (confidence interval) and the level of statistical significance.
|
One day
|
|
Establishment of a biobank
Časové okno: One day
|
Establishment of a biobank
|
One day
|
Spolupracovníci a vyšetřovatelé
Sponzor
Vyšetřovatelé
- Vrchní vyšetřovatel: Sophie TROUILLET-ASSANT, Laboratoire Commun de Recherche, Hôpital Lyon Sud, Hospices Civils de Lyon, France
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další identifikační čísla studie
- 69HCL26_0579
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
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