bacterial infectious diseases
Conditions
Interventions
None listed
Sponsors
Canisius Wilhelmina Ziekenhuis
Eligibility
Age
2 Years to 17 Years
Inclusion criteria
Inclusion criteria: 1. Patients who receive intravenous treatment with amoxicillin 2. Patients
Exclusion criteria
Exclusion criteria: Patients with a known allergy to amoxicillin or related compounds
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary parameters in this study will be: * T1/2 (half-life during elimination phase) and Vss (volume of distribution in steady state) of amoxicillin * Total body clearance, AUC (area under the time-concentration curve), MRT (mean residence time) Interpretation of pharmacokinetic parameters * Plasma concentrations and the AUC*s of amoxicillin will be compared to the MIC (minimal inhibitory concentration) of the microbe to be eliminated. * T1/2 of amoxicillin will be related to the GFR (glomerular filtration) * All pharmacokinetic parameters will be related to the personal characteristics of the subjects Finally, all data will lead to a new dosing advice on intravenous amoxicillin treatment in children. | — |
Countries
Netherlands
Outcome results
None listed