Pharmacokinetics Vancomycin CVVHDF with OXiris Membrane

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMahidol University

About this trial

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.

Eligibility criteria

Qualifiers

Patients aged more than 18 years.

Admitted to the intensive care unit of Ramathibodi Hospital.

Under continuous renal replacement therapy (CRRT) with CVVHDF using oXiris filter.

Received vancomycin at least once after starting CRRT with CVVHDF using oXiris filter.

Disqualifiers

Patients with a history of vancomycin allergy.

Patients expected to die within 24 hours after inclusion in study.

Patients with circuit clotting occurring more than 2 hours during the blood draw period.

Patients treated with extracorporeal membrane oxygenation (ECMO).

Trial design

Treatments tested in this trial

  • Vancomycin

Treatment groups

8 Participants
are divided into 1 treatment group

Sponsors and collaborators