Infective Endocarditis Clinical Trial
— NESSIEOfficial title:
NExt-Generation Sequencing and Cell Culture-based Characterization of S. Aureus in Infective Endocarditis
NCT number | NCT04257292 |
Other study ID # | 01 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | September 1, 2019 |
Est. completion date | July 31, 2020 |
Infective endocarditis is a deadly disease with a mortality rate between 20 and 40%.
Antibiotic therapy is of utmost importance. It is primarily guided by microbial results from
positive blood culture. However, culture-based microbiological diagnostic can identify the
species, but not the strain or the genotypic characteristics of a pathogen. Identifying the
strain can be of utmost clinical significance. S. aureus is the most common causative
organism of IE worldwide (16%-32%). This pathogen causes massive valve destruction and
abscesses, which is strongly dependent on the expression of virulence factors that vary
between different S. aureus strains.
Functional characterization of S. aureus and determination of virulence factors can currently
be achieved through cell culture-based assays (CCBA). However, these tests are very time
consuming and cannot be performed as routine clinical diagnostics. Next Generation Sequencing
(NSG) has the potential to identify the genotypic characteristics of the pathogen, which is
important to determine its virulent potential.
The aim of this study is to evaluate the possible utilization of NGS in the prediction of
virulence factors of S. aureus and to compare it to the virulence factors determined using
CCBA.
Hopefully, by comparing the NGS and CCBA, the investigators will get a faster way of
determining the possible virulence factors. The NGS method can be further utilized to
describe the prevalence of different strains of bacteria in infected valve tissue and blood
culture samples. The collected data will serve as a basis for further evaluation of the
potentials of NGS-based Diagnosis of IE, as well as a comparison between NGS-guided
antibiotic treatment and the standard of care antibiotic treatment.
Status | Recruiting |
Enrollment | 10 |
Est. completion date | July 31, 2020 |
Est. primary completion date | February 28, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - patients with the diagnosis infective endocarditis and indication for heart surgery on a heart valve - signed informed consent - age =18 years - pathogens (S. aureus) can be isolated from blood culture AND from the removed valve tissue Exclusion Criteria: - S. aureus can not be isolated from removed valve tissue |
Country | Name | City | State |
---|---|---|---|
Germany | Jena University Hospital, Clinic for Cardiothoracic surgery | Jena |
Lead Sponsor | Collaborator |
---|---|
Jena University Hospital | Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | biofilm growth | ability of S. aureus strains isolated from the blood and heart tissue of included patients to build a biofilm | through study completion (about 1 year) | |
Secondary | invasion characteristics | characteristics of the S. aureus strains isolated from the blood and heart tissue of included patients to invade other cells (host cell invasion; persistence in host cells; tests will be conducted in cell culture) | through study completion (about 1 year) | |
Secondary | adhesion characteristics | characteristics of the S. aureus strains isolated from the blood and heart tissue of included patients to adhere to other human cells (important information regarding the ability to attach to heart tissue; test will be conducted in cell culture) | through study completion (about 1 year) | |
Secondary | toxine production | characteristics of the S. aureus strains isolated from the blood and heart tissue of included patients regarding production of toxins which will lead to information about induction of inflammation processes and induction of host cell death | through study completion (about 1 year) |
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