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Investigation of immune responses against Staphylococcus aureus * analysis of antibodies and antibody producing cells in patients with Staphylococcus aureus infections and patients whose wounds are colonised by Staphylococcus aureus

Investigation of immune responses against Staphylococcus aureus * analysis of antibodies and antibody producing cells in patients with Staphylococcus aureus infections and patients whose wounds are colonised by Staphylococcus aureus - AntiStaph

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33490
Enrollment
120
Registered
2009-11-16
Start date
2009-12-08
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

hospital infections S. aureus colonization and infection

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Provision of written informed consent and history of S. aureus infection, presence of toxin producing strains or wound colonisation

Exclusion criteria

Exclusion criteria: 1. A history of, or presence of diseases or other conditions in which no blood donation can take place (as judged by the investigator or the treating physician). 2.Evidence of having serum hepatitis or carrying the hepatitis B surface antigen or Hepatitis C antibodies or being HIV positive. 3. Abuse of alcohol or drugs or any other condition. 4. Pregnancy. 5. Positive drug screen for Benzodiazepines, methadone, metamphetamine, morphine, PCP, tricyclic antidepressants, amphetamines, cocaine, cannabinoids, barbiturates and ethanol 6. Subjects, who in the opinion of the investigator or the treating physician should not, for reasons of safety, participate in the study.

Design outcomes

Primary

MeasureTime frame
The primary study parameter is a detectable IgA or IgG response against staphylococcal antigens relevant for the development of therapeutic antibodies. The endpoint will be defined by the absence of a detectable IgA or IgG response against antigens relevant for the development of therapeutic antibodies.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)