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Absorption of tobramycin from the gut in critically ill patients treated with selective decontamination of the digestive tract (SDD)

Absorption of tobramycin from the gut in critically ill patients treated with selective decontamination of the digestive tract (SDD) - Absorption of tobramycin during SDD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30143
Enrollment
20
Registered
2006-10-30
Start date
2006-10-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

antibiotics permeability

Interventions

None listed

Sponsors

Onze Lieve Vrouwe Gasthuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Critically ill patients acutely admitted to the intensive care patients, treated with selective decontamination of the digestive tract for at least 24 hours.

Exclusion criteria

Exclusion criteria: Intravenous use of tobramycin or gentamycin

Design outcomes

Primary

MeasureTime frame
concentrations of tobramycin in blood excretion of tobramycin in urine

Secondary

MeasureTime frame
renal function SOFA score APACHE score

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)