An exploratory single-center, cross-sectional study for the characterisation of human variability in toxicodynamics: towards the development of quantitative adverse outcome pathways.
- Conditions
- iet van toepassing betreft karakterisering van de menselijke variabiliteit in de toxicodynamiekN.a.
- Registration Number
- NL-OMON56742
- Lead Sponsor
- niversiteit Leiden
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
Signed informed consent.
Male or female subjects, 20 - 69 years of age
In general, stable good health.
Exclusion Criteria
Loss or donation of blood over 500mL within three months prior to screening.
Alcohol consumption in the 24 hours preceding the study visit, or not being in
fasted state 4 hours preceding the study visit (water is allowed).
Smoking in the 4 hours preceding the study visit.
(A history of) any clinically significant medical condition, factor or
abnormality that might interfere with study conduct or interpretation, as
judged by the investigator.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method