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Carriage of S. aureus and interaction with the nasal microbiome

Carriage of S. aureus and interaction with the nasal microbiome - MACOTRA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON48845
Enrollment
70
Registered
2018-06-20
Start date
2019-02-09
Completion date
Unknown
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

S. aureus carriage

Interventions

After inclusion and determination of carrier status, all volunteers will be treated with Mupirocin (Bactroban) 2% nasal ointment and Chlorhexidine gluconate (Hibiscrub®) 4% cutaneous body wash solut

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Volunteers must be over 18 years old

Exclusion criteria

Exclusion criteria: - Employee of the Erasmus MC - Intermittent carrier of Staphylococcus aureus - Use of drugs influencing microbiome in 3 months prior to the study period i.e. antibiotics, antiparasitics or antifungals - Regular use of commercial probiotics in 3 months prior to the study period - Known allergy to components of the intervention treatment (see Ch 5.1) - Pregnant and breastfeeding women, due to limited scientific evidence on adverse effects of mupirocin treatment during pregnancy and breastfeeding. - Known chronic diseases affecting the immune system (such as diabetes mellitus, renal insufficiency, COPD, heart diseases, immunocompromised status (HIV, AIDS), skin diseases such as severe eczema or use of immunosuppressant drugs

Design outcomes

Primary

MeasureTime frame
Microbiome composition of the nose, to be analysed in relation to S. aureus carrier status and decolonization.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)