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UnknownNCT06261164

Population Pharmacokinetic Model of Amikacin and Vancomycin in Critically Ill Patients

Development and Use of a Population Pharmacokinetic Model of Amikacin and Vancomycin for the Optimization of Dosing Regimens in Critically Ill Patients on Different Modalities of Extracorporeal Hemoadsorption

Status
Unknown
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
University Clinical Centre of Republic of Srpska · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The object of the scientific research is the characterization of the pharmacokinetic profile and the investigation of factors of pharmacokinetic variability of amikacin and vacnomycin in critically ill patients with a diagnosis of sepsis-like condition (SIRS), hospital-acquired sepsis and/or septic shock and who are on extracorporeal therapy with Cytosorb® and Oxiris® adsorbents.

Conditions

Interventions

TypeNameDescription
DEVICECytosorb® and Oxiris® adsorbentsThe pharmacokinetic profile and the investigation of factors of pharmacokinetic variability of amikacin and vacnomycin in critically ill patients with a diagnosis of sepsis-like condition (SIRS), hospital-acquired sepsis and/or septic shock and who are on extracorporeal therapy with Cytosorb® and Oxiris® adsorbents.

Timeline

Start date
2024-01-31
Primary completion
2024-12-31
Completion
2025-01-31
First posted
2024-02-15
Last updated
2024-02-15

Locations

1 site across 1 country: Bosnia and Herzegovina

Source: ClinicalTrials.gov record NCT06261164. Inclusion in this directory is not an endorsement.

Population Pharmacokinetic Model of Amikacin and Vancomycin in Critically Ill Patients (NCT06261164) · Clinical Trials Directory