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
- Conditions
- hospital infectionsS. aureus colonization and infection1000401810040785
- Registration Number
- NL-OMON33490
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
Provision of written informed consent and history of S. aureus infection, presence of toxin producing strains or wound colonisation
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.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary study parameter is a detectable IgA or IgG response against<br /><br>staphylococcal antigens relevant for the development of therapeutic antibodies.<br /><br>The endpoint will be defined by the absence of a detectable IgA or IgG response<br /><br>against antigens relevant for the development of therapeutic antibodies.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Not applicable</p><br>