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RECRUITING
NCT06543940
NA

Pharmacokinetics Vancomycin CVVHDF with OXiris Membrane

Sponsor: Mahidol University

View on ClinicalTrials.gov

Summary

This study is a general pharmacokinetic investigation of vancomycin in patients receiving continuous veno-venous hemodiafiltration (CRRT) with the oXiris membrane. This membrane offers the added benefit of absorbing inflammatory cytokines. In vitro studies show that vancomycin is reduced by around 20 percent in patients using the AN69ST membrane, which is part of the oXiris membrane's structure. However, there is currently a lack of in vivo studies demonstrating the impact of the oXiris membrane on vancomycin levels. Therefore, the hypothesis of this study is that vancomycin is also reduced by absorption in the oXiris membrane. This study measures the levels of vancomycin in these patients to determine the pharmacokinetic parameters.

Official title: Pharmacokinetics of Vancomycin in Patients Receiving Continuous Veno-Venous Hemodiafiltration (CVVHDF) with the Absorptive OXiris Membrane

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

8

Start Date

2024-09-01

Completion Date

2025-12-31

Last Updated

2025-01-24

Healthy Volunteers

No

Interventions

DRUG

Vancomycin

vancomycin dose is 7.5 to 10 mg/kg

Locations (1)

Facullty of Pharmacy Mahidol University

Bangkok, Payathi, Thailand