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DOSING AND PHARMACOKINETICS OF INTRAVENOUS AMOXICILLIN IN CHILDREN

DOSING AND PHARMACOKINETICS OF INTRAVENOUS AMOXICILLIN IN CHILDREN - dosing/pharmacokinetics of intravenous amoxicillin in children

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32761
Enrollment
70
Registered
2010-02-17
Start date
2010-12-01
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

bacterial infectious diseases

Interventions

None listed

Sponsors

Canisius Wilhelmina Ziekenhuis
Lead Sponsor

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

MeasureTime 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

Source: NL-OMON (via WHO ICTRP)