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RecruitingNCT06594250RISTAUpdated Nov 6, 2026

Study of the Nasal Intracellular Reservoir of Staphylococcus Aureus in Patients With S. Aureus Bacteremia

An observational study in Bacteria Infection Mechanism, sponsored by Centre Hospitalier Universitaire de Saint Etienne. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Centre Hospitalier Universitaire de Saint Etienne · Observational

From the registry’s dates

  • Started Sep 2024; still recruiting 2 years 2 months later.
Updated Nov 6, 2026Primary completion movedStudy completion moved+2 moreGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
405
Ages
18 Years and older
Sex
All
01

Study summary

Staphylococcus aureus bacteremia is a serious infection associated with a high mortality rate (with or without associated infective endocarditis (IE)), long hospital stays and multiple complications, due to the terrain in which it occurs and its secondary localization. They may be community-acquired or healthcare-associated infections. Being a carrier of S. aureus is a known risk factor for S. aureus bacteremia. Although several mucosal sites of carriage have been described, screening for carriage is most often carried out at the nasal level, both for reasons of simplicity and because it is the predominant site of carriage of this bacterium. However, S. aureus carriage is a frequent occurrence, affecting around 1/3 of the general population.

Read the detailed description

Long considered an extracellular bacterium, the investigators now know that S. aureus can have an intracellular reservoir. This was initially described in situations of infection (bone infections, vascular infections) and more recently in situations of nasal carriage without associated infection. Among S. aureus carriers, between 15% and 30% have an intracellular reservoir of this bacterium, depending on the study, in patients with no S. aureus infection. For S. aureus carriers with S. aureus infection, there are no data in the literature. The clinical significance of this intracellular reservoir in a carrier situation is currently unknown. The study team was able to demonstrate in vitro that this reservoir was not affected by the mupirocin used in decolonization, and preliminary results suggest that in vivo this reservoir may also be associated with decolonization failure.

Moreover, in vitro, it has been suggested that S. aureus may act on autophagy to promote intracellular survival. Is the intracellular reservoir more frequent in patients with S. aureus bacteremia? Is it associated with a poorer prognosis in S. aureus bacteremia? Is it associated with the production of certain S. aureus intracellular persistence factors? Is it associated with a slowdown in autophagic flow in nasal cells or phagocytes? These questions remain unanswered to this day.

To explore these questions, the investigators plan to conduct a study to assess the frequency of the intracellular S. aureus reservoir (within carriers) in S. aureus bacteremia and in bacteremia to another pathogen (control group). They would also like to study the impact of this reservoir on the persistence of carriage and prognosis (death, duration of bacteremia, length of stay, presence of secondary localizations of bacteremia or endocarditis in the case of S. aureus bacteremia).

02

Conditions studied

  • Bacteria Infection Mechanism

Keywords

  • Staphylococcus aureus bacteremia
03

In context

Lead sponsor

Centre Hospitalier Universitaire de Saint Etienne is the lead sponsor of 597 studies on the registry; 127 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients treated at St-Etienne University Hospital with bacteremia with or without IE. Patients will be assigned to the experimental group in the case of S. aureus bacteremia (whether or not associated with an IE), or to the control group in the case of bacteremia caused by a pathogenic bacterium other than S. aureus (whether or not associated with an IE).

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Bacteremia
  • Patient affiliated or entitled to a social security plan
  • Patient who has signed a consent form to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Antibiotic therapy in place for more than 5 days at the time of inclusion
  • Nasal decolonization of S. aureus within 12 months
  • Pregnant or breast-feeding women
  • Patients under guardianship
  • Polymicrobial bacteremia including S. aureus
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
405 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Experimental group

    Experimental group comprising patients with S. aureus bacteremia with or without IE

    Diagnostic Test: Nasal swab · Biological: Venous sampling · Biological: Antibiotic treatment · Device: Nasal swab · Biological: Intracellular reservoir test

  • Control group

    Control group comprising patients with bacteremia with a pathogenic bacterial species other than S. aureus with or without IE.

    Diagnostic Test: Nasal swab · Biological: Venous sampling · Biological: Antibiotic treatment · Device: Nasal swab · Biological: Intracellular reservoir test

Interventions

  • Diagnostic testNasal swab

    Nasal swab to detect nasal carriage of S. aureus

  • BiologicalVenous sampling

    Peripheral venous sampling to collect peripheral blood mononuclear cells.

  • BiologicalAntibiotic treatment

    Antibiotic treatment for bacteremia (+/- 1 month), in all patients with S. aureus

  • DeviceNasal swab

    A new nasal swab will be taken using the same technique, to see whether or not the carriage persists

  • BiologicalIntracellular reservoir test

    In the event of positive carriage, a new intracellular reservoir test will be performed. A search for relapse (new S. aureus infection) or recurrence (S. aureus bacteremia if the 1st bacteremia was due to another pathogen) will be carried out.

06

What researchers measure

Primary outcomes

  1. Number of intracellular S. aureus carriers at nasal level research

    Number of intracellular S. aureus carriers at nasal level research in patients with S. aureus bacteremia associated or not

    Time frame: At inclusion

Secondary outcomes

  1. Number of intracellular S. aureus carriers at nasal level research

    Time frame: Day 7

  2. In-hospital mortality rate (%)

    In-hospital mortality rate directly related to infection (septic shock, multivisceral failure, death during surgical management related to infection) during bacteremia

    Time frame: Month 1

  3. Mean duration of S. aureus bacteremia (Day)

    Time frame: Month 1

  4. Average number of secondary localizations of S. aureus bacteremia

    Clinically diagnosed, or on examination carried out as part of the extension work-up performed as part patient management (Scan, echocardiography, scintigraphy, etc.)

    Time frame: Month 2

  5. Average length of stay in hospital for S. aureus bacteremia (Day)

    Time frame: Month 1

  6. Proportion of nasal S. aureus carriers still carriers at the end of treatment for bacteremia (%)

    Time frame: Month 1

  7. Proportion of nasal S. aureus carriers still carriers one year after the end of treatment for bacteremia (%)

    Time frame: Month 12

07

Study locations

1 of 1 sites recruiting
  • Centre Hospitalier Universitaire de St Etienne
    Saint-Etienne, 42055, France
    Recruiting
    • Elisabeth BOTELHO-NEVERS, MD-PhD · Principal investigator
    • Amadine GAGNEUX-BRUNON, MD-PhD · Sub investigator
    • Léo SAUVAT, MD · Sub investigator
08

Updates

1 registry update since Sep 25, 2026
Sites
1 site added, 1 site removed
Show site
  • Centre Hospitalier Universitaire de St Etienne · Saint-Etienne, France
Show 1 removed
  • Centre Hospitalier Universitaire de St Etienne · Saint-Étienne, France
Nov 6, 2026
Primary completion
Nov 2025→Nov 2027
Nov 6, 2026
Study completion
Nov 2025→Nov 2027
Nov 6, 2026
Show all 1 update
  1. Nov 6, 2026
    1 site added, 1 site removed
    Show site
    • Centre Hospitalier Universitaire de St Etienne · Saint-Etienne, France
    Show 1 removed
    • Centre Hospitalier Universitaire de St Etienne · Saint-Étienne, France
    Primary completion Nov 2025→Nov 2027
    Study completion Nov 2025→Nov 2027
    + 3 other changes: verification date, contact details and index terms

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT06594250
Responsible party
Sponsor
First posted
Sep 19, 2024
Start date
Sep 2, 2024
Primary completion
Nov 2027 (estimated)
Completion
Nov 2027 (estimated)
Last update
Nov 6, 2026

Study contacts

Elisabeth BOTELHO-NEVERS, MD-PhD
Contact
elisabeth.botelho-nevers@chu-st-etienne.fr
(0)477120764 ext. +33
Amandine Gagneux-Brunon, MD-PhD
Contact
amandine.gagneux-brunon@chu-st-etienne.fr
(0)477120356 ext. +33
Elisabeth BOTELHO-NEVERS, MD-PhD
principal investigator · Centre Hospitalier Universitaire de Saint Etienne
Léo SAUVAT, MD
study chair · Centre Hospitalier Universitaire de Saint Etienne

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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