Clinical trial Recruiting at 1 site Interventional Ages 80 and up

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 typeInterventional
Ages80 Years and up
SexAll
Enrollment62 (estimated)
SponsorHospices Civils de Lyon
Academic / other
Locations1 site (Villeurbanne)
StatusRecruiting
StartedDecember 2, 2025
Main results expectedDecember 3, 2026
Study endsDecember 3, 2026
Registry record updatedApril 8, 2026
Trial IDNCT07239830 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

  • Hôpital des Charpennes (Hospices Civils de Lyon)
    Villeurbanne, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.