Trials / Completed
CompletedNCT04781569
Staphylococcus Aureus Caught in Action at the Site of Infection
A Single Centre, Unblinded, Prospective Cohort Study Identifying Pathogen Adaptations in Patients Suffering From Invasive S. Aureus Infection Compared to Colonized, Healthy Individuals
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- University Hospital, Basel, Switzerland · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
This study is to obtain a comprehensive view of S. aureus adaptations in the infected human host and (i) to improve the understanding of the interface between antibiotic therapy, resistance development and virulence factor adaptation in S. aureus infected patients, and (ii) to adapt these findings into a more sustainable use of antimicrobials for therapy.
Detailed description
Staphylococcus (S.) aureus is notorious for its ability to develop resistance. This study is to obtain a comprehensive view of S. aureus adaptations in the infected human host and (i) to improve the understanding of the interface between antibiotic therapy, resistance development and virulence factor adaptation in S. aureus infected patients, and (ii) to adapt these findings into a more sustainable use of antimicrobials for therapy. Patients with S. aureus infections who will routinely undergo diagnostic and surgical procedures will be identified. Intraoperative samples from the site of infection during surgery will be taken. Additionally, two blood drawing events (22.5ml in total) will be performed and nose swabs will be taken. The biological material will be analysed. This project will be the first to study different phenotypes of invasive S. aureus directly from its environment in vivo.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | data collection | Health-related personal data such as year of birth, sex, Body Mass Index (BMI), infection classification, concomitant infections, comorbidities according to medical chart, standard diagnostic markers (CRP, blood differential plots, creatinine, ...), medication, treatment start, treatment end and discharge from hospital will be collected. |
| DIAGNOSTIC_TEST | blood draw | 2 blood drawing events (in total 22.5 ml) will be performed in the patient. 1 blood drawing events will be performed in the healthy proband. |
| DIAGNOSTIC_TEST | nose swabs | 2 nose swabs will be taken in the patient. 1 nose swab will be performed in the healthy proband. |
| DIAGNOSTIC_TEST | Intraoperative tissue samples | Intraoperative tissue samples from the site of infection during surgery will be taken in the patient. |
Timeline
- Start date
- 2017-06-06
- Primary completion
- 2020-11-23
- Completion
- 2020-11-23
- First posted
- 2021-03-04
- Last updated
- 2021-06-03
Locations
1 site across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT04781569. Inclusion in this directory is not an endorsement.