Pharmacokinetics of Daptomycin in Critically Ill Patients Receiving Continuous Venovenous Hemodialysis (CVVHD)

Completed · Phase 4

Conditions studied: Critically Ill, Hemodialysis

In brief

Daptomycin is an antibiotic that is affective against many strains of antibiotic resistant microorganisms. This antibiotic would be appropriate for use in the intensive care unit (ICU) considering the severity of illness and high risk for infection within this hospital environment. While in the ICU, patients may develop acute renal failure. Approximately 75% of ICU patients who develop acute renal failure will require some form of renal replacement therapy until their kidneys recover. Continuous hemodialysis is becoming one of the most common forms of dialysis in the ICU as it is a gentle type of dialysis provided over longer periods of time. The current data demonstrating the ability of continuous hemodialysis to remove daptomycin from the body is derived from in-vitro trials. The purpose of this trial is to determine the extent of daptomycin removal from critically ill patients receiving continuous hemodialysis. Findings from this trial will be used to develop new dosing recommendations for daptomycin in continuous hemodialysis.

Key facts

Study ID

NCT00663403

Run by

University of Michigan

People needed

8

Starts

2007-02-01

Expected to finish

2009-04-01

Last updated by the study team

2015-12-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• =/> 18 years of age
• Prescribed Continuous Venovenous Hemodialysis (CVVHD) as determined by the primary physician
• Prescribed daptomycin as determined by the primary physician
• Informed consent granted

You may not qualify if…

• < 18 years of age
• Allergy to daptomycin
• Patients being primarily treated with daptomycin for diagnosis of osteomyelitis, meningitis, or pneumonia without adequate concomitant use of other more effective antimicrobial agents as daptomycin is not indicated for primary treatment of these types of infections
• Inability to complete 48 hours of Continuous Venovenous Hemodialysis (CVVHD)
• Concurrent use of other extracorporeal therapies such as Extracorporeal Membrane Oxygenation (ECMO) or plasmapheresis and intermittent hemodialysis
• Inability to obtain informed consent
• Pregnant and/or breastfeeding women

Where it is running

• University of Michigan University Hospital — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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