Interferon reference for older people (REFIPA)
Official title: Reference Values Determination of Nasal and Blood Interferon Scores in Uninfected Older Subjects REFérence Interféron Older Subjects (Older People Interferon Reference) - REFIPA Study
Run by Hospices Civils de Lyon · NCT07239830 · Data updated 2026-11-12
This project will test whether measuring type I interferon responses can help identify active respiratory virus infections in people aged 80 and over.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 80 Years and up |
| Sex | All |
| Enrollment | 62 (estimated) |
| Sponsor | Hospices Civils de Lyon Academic / other |
| Locations | 1 site (Villeurbanne) |
| Status | Recruiting |
| Started | December 2, 2025 |
| Main results expected | December 3, 2026 |
| Study ends | December 3, 2026 |
| Registry record updated | April 8, 2026 |
| Trial ID | NCT07239830 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are community-dwelling adults aged 80 or older who live in the Lyon metropolitan area, weigh at least 45 kg, have no symptoms of active infection, and do not have autoimmune disorders affecting interferon.
✕Probably not a fit
People with current symptoms of infection, known autoimmune interferon disorders, those enrolled in conflicting interventional studies, or those living outside the Lyon metropolitan area are unlikely to be eligible or receive benefit from participating.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The project will recruit adults aged 80 and older without symptoms of active infection at Hôpital des Charpennes in Villeurbanne to collect blood samples and basic clinical information. Researchers will measure type I interferon levels and related immune markers to define baseline interferon response ranges in this age group. Those reference data will be compared with known patterns of active viral replication to determine whether interferon signals distinguish active from past infections. The goal is to develop a host-based diagnostic marker that complements PCR detection of viral genetic material.
Why it matters
Potential benefit: If successful, this approach could help clinicians tell whether a detected respiratory virus is actively replicating, reducing missed diagnoses and unnecessary treatments or isolation.
How similar studies have gone: Previous research has shown that interferon and other host immune signatures can indicate viral infection in younger populations, but building specific reference ranges for very old adults is a relatively novel focus.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subject aged 80 or over * Patient admitted to the Charpennes hospital day unit or outpatient clinic for follow-up OR accompanying patient who receive care at the Charpennes geriatric hospital OR subject recruited through the local press * Weight greater than or equal to 45 kg * Subject living in the Lyon metropolitan area Exclusion Criteria: * Subjects with symptoms of active infection (symptom questionnaire or temperature \> 37.5°C). * Subjects with an autoimmune disease linked to a dysregulated interferon response. * Subjects participating in another interventional study involving an exclusion period that is still ongoing or that may interfere with the present protocol. * Subjects deprived of their liberty by judicial or administrative decision * Subjects receiving psychiatric care * Adults subject to legal protection measures (guardianship, curatorship) * Subjects not affiliated with a social security scheme or beneficiaries of a similar scheme
Where it's running
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Hôpital des Charpennes (Hospices Civils de Lyon)
Villeurbanne, France Recruiting
Study contacts
- Study coordinator: Antoine GARNIER-CRUSSARD
- Email: antoine.garnier-crussard@chu-lyon.fr
- Phone: +33 4 72 43 20 50
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.