Clinical trial Recruiting at 1 site Observational

Investigating genetic factors in severe infections

Official title: Genetic Susceptibility to Severe Infections Including in Particular But Not Exhaustively All Types of Viral, Bacterialn and Fungal Infections.

Run by Institut National de la Santé Et de la Recherche Médicale, France · NCT06102070 · Data updated 2026-11-12

This study is trying to find out if certain genes make some people more likely to get severe infections than others by looking at patients with rare and serious infections.

Quick facts

Study typeObservational
SexAll
Enrollment2000 (estimated)
SponsorInstitut National de la Santé Et de la Recherche Médicale, France
Government
Locations1 site (Paris, Île-de-France Region)
StatusRecruiting
StartedFebruary 18, 2022
Main results expectedFebruary 17, 2037
Study endsOctober 18, 2038
Registry record updatedJuly 7, 2026
Trial IDNCT06102070 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals with proven rare and severe infections who are hospitalized or followed in specialized medical settings.

Probably not a fit

Patients with acquired immunodeficiency or those who are pregnant may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to explore the genetic susceptibility of individuals to severe infections by examining the interplay between genetic and environmental factors that influence immune responses. It will involve recruiting patients with rare and severe infections, focusing on those requiring hospitalization or experiencing chronic infections. Blood samples and skin biopsies will be collected to analyze the underlying genetic factors contributing to these infections. The study seeks to enhance understanding of why some individuals develop severe disease while others do not.

Why it matters

Potential benefit: If successful, this study could lead to improved identification of individuals at risk for severe infections and inform targeted prevention strategies.

How similar studies have gone: While the investigation of genetic susceptibility to infections has been explored, this specific approach focusing on rare infections is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* to sign the informed consent signed by the patient. In the case of a minor patient, consent is signed by the holders of parental authority. In the case of a protected adult patient, the consent is signed by their legal representative. In the case of an adult patient unable to consent at the time of inclusion, consent is signed by a family member.
* to have a proven rare and severe infection
* to be hospitalized or followed in a specialized hospital department, in the emergency room or in intensive care
* to be affiliated to the French Social Security system
* for relatives, to be related to the index case up to the 3rd degree: Parents, Children, Brother, Sister, Grandparents, Uncles, Aunts, Cousins, Nephews, Nieces

Exclusion Criteria

* to have an acquired immunodeficiency (having received immunosuppressive treatment in the 3 months preceding the onset of the disease or being HIV positive)
* pregnant woman at the time of illness

Where it's running

  • Centre d'Etudes des Déficits Immunitaires (CEDI), Hôpital Necker-Enfants
    Paris, Île-de-France Region, France
    Recruiting

Study contacts

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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.