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Study of Ceftazidime-Avibactam Blood Concentrations in Intensive Care Unit Patients With Renal Failure Requiring Continuous Dialysis

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Temple University

Status

Unknown

Conditions

Renal Failure
Critical Illness
Bacterial Infections

Treatments

Drug: Ceftazidime-avibactam

Study type

Observational

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

The study's primary objective is to determine plasma and dialysis fluid concentrations in patients prescribed ceftazidime-avibactam as the standard treatment for their infection and requiring continuous venovenous hemodiafiltration (CVVHDF) as part of the standard treatment for acute or chronic renal failure. Secondarily, the study will evaluate the pharmacokinetics of ceftazidime-avibactam in these patients on CVVHDF. The study will also determine if the prescribed dose meets pharmacodynamic targets.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults > 18 years of age
  • Patients requiring continuous renal replacement therapy (CRRT) due to acute or chronic renal failure
  • documented or suspected infection requiring a prescription for ceftazidime-avibactam

Exclusion criteria

  • Patients on CRRT < 24 hours
  • Patients on ceftazidime-avibactam < 24 hours
  • Patients unable to remain on CRRT for 32 hours continuously without clotting

Trial design

10 participants in 1 patient group

Ceftazidime and Avibactam
Description:
Ceftazidime-avibactam pharmacokinetic monitoring
Treatment:
Drug: Ceftazidime-avibactam

Trial contacts and locations

1

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Central trial contact

Christina Rose, Pharm.D.; Daniel Mueller, MD

Data sourced from clinicaltrials.gov

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