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Modelling of saliva gentamicin concentrations in neonates receiving gentamicin treatment

Modelling of saliva gentamicin concentrations in neonates receiving gentamicin treatment - Saliva gentamicin concentration in neonates

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48679
Enrollment
60
Registered
2018-08-27
Start date
2018-10-08
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

antibiotic treatment

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: Gentamicin treatment Admission to the neonatology ward , pediatrics/pediatric surgery department, obstetrics department or maternity ward of the AMC/Juliana children*s hospital (Haga Hospital) Signed informed consent from both parents prior to any study-mandated procedure

Exclusion criteria

Exclusion criteria: Congenital disease of the salivary glands Parent refusal Inability to sample saliva

Design outcomes

Primary

MeasureTime frame
Primary study paramters are the saliva gentamicin concentrations at different time-points.

Secondary

MeasureTime frame
Secundary study parameters of this study are gentamicin concentrations in plasma, correlation between plasma and saliva gentamicin, citric acid stimulation during saliva sampling (Y/N), sampling duration, salivary pH and sample volume.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)