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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03374371
Other study ID # NI17029J
Secondary ID 2017-A02742-51
Status Completed
Phase
First received
Last updated
Start date March 1, 2018
Est. completion date December 18, 2020

Study information

Verified date December 2021
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to identify biomarkers allowing the distinction between invasive and non-invasive strains of Staphylococcus epidermidis. This distinction is important to determine if the patient is infected and, as a consequence, if an antibiotic treatment is required.


Description:

In the hospital, a large proportion of bacteraemia and implantable medical device infections are caused by Staphylococcus epidermidis. This microorganism is the most abundant on human skin and all patients are carriers. Its remarkable ability to form biofilms on most materials explains that catheter-related infections are by far the most common. S. epidermidis infections are difficult to treat because most strains are multi-resistant and antibiotics are less effective in the presence of biofilms. In addition, S. epidermidis poses a major diagnostic problem because it is also the first source of contamination of blood culture sample and intraoperative samples (in case of suspected infection of orthopedic material in particular). Thus, when a sample is positive for S. epidermidis, there is less than a 25% chance that it reflects true bacteremia in the patient and 30% of patients would inappropriately receive vancomycin following contaminated blood cultures. Differentiating a contamination of a blood or intraoperative sample from true S. epidermidis infection is therefore crucial for patient management because unnecessary antibiotic therapy is potentially responsible for the emergence of resistant strains, toxicity and additional costs. The objective of this study is to identify the genetic markers that make it possible to differentiate the strains causing infections from the strains causing contamination by comparing their genomes using high throughput sequencing.


Recruitment information / eligibility

Status Completed
Enrollment 320
Est. completion date December 18, 2020
Est. primary completion date December 18, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: CASE Inclusion Criteria: Population 1: nosocomial bacteraemia associated with intravascular devices 1. Hospitalized patient with intravascular device (peripheral or central, venous or arterial, short or long duration) for at least 48 hours before the development of bacteraemia 2. Presenting a definite infection with S. epidermidis according to the categorization criteria, Sub-Population 1A: 3a) Aged less than 28 days (New-born) Sub-population 1B: 3b) Aged 28 days or more Population 2: nosocomial infections of implanted material 1. An operated patient carrying implanted equipment following orthopaedic surgery, following cardiac surgery or following neurosurgery, 2. Presenting a definite infection with S. epidermidis according to the categorization criteria occurring in the year following surgery CONTROL Inclusion Criteria: Population 1: carrier of intravascular devices 1. Hospitalized patient with intravascular device (peripheral or central, venous or arterial, short or long duration) for at least 48 hours before positive blood culture with S. epidermidis 2. Certain contamination with S. epidermidis according to the categorization criteria, Sub-Population 1A: 3a) Aged less than 28 days (Newborn) Sub-population 1B: 3b) Aged 28 days or more Population 2: carrier of implanted material 1. An operated patient carrying implanted equipment following orthopedic surgery, following cardiac surgery or following neurosurgery, 2. Presenting a certain contamination to S. epidermidis according to the categorization criteria occurring in the year following surgery Exclusion Criteria: CASE Exclusion Criteria Population 1: nosocomial bacteremia associated with intravascular devices 1. Opposition of the patient or the holders of parental authority (minor patients) 2. Patient with polymicrobial infection 3. Patient with a colonized catheter (positive catheter end culture <103UFC / mL) with no clinical signs of local or general infection and with sterile peripheral blood cultures 4. Patient with local catheter infection (positive catheter end culture> 103UFC / mL) with local inflammatory signs only and with sterile peripheral blood cultures Population 2: nosocomial infections of implanted material 1. Opposition of the patient or the holders of parental authority (minor patients) 2. Patient with an infection of material concomitant with a catheter-related infection CONTROL Exclusion Criteria Populations 1 and 2: Opposition of the patient or the holders of parental authority (minor patients)

Study Design


Related Conditions & MeSH terms

  • Staphylococcus Epidermidis Positive Blood Culture

Intervention

Diagnostic Test:
high-throughput sequencing
technique of high-throughput sequencing of the markers present in the genome of the S. epidermidis strains responsible for infection in order to help to discriminate the true infections of the contaminations

Locations

Country Name City State
France Hôpital Necker Enfants Malades Paris Ile De France

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary genetic markers of S. epidermidis to identify genetic markers associated with a significant risk of invasive S. epidermidis infections at the time of the positive sampling of S. epidermidis
Secondary Correlation of the genotype with the characteristics of the infections identification of genetic markers specifically associated with a type of infection (catheter-related bacteremia in newborns, catheter-related bacteremia in patients 28 days or older, infections of orthopedic equipment or infections of cardiac equipment) at the time of the positive sampling of S. epidermidis
Secondary Intra-hospital cross-transmission detection The comparison of the strains will be based on the study of the variations in the part of the genome that is common to all the strains to detect possible transfers between patients at the time of the positive sampling of S. Epidermidis