CompletedPhase 4ACTRN12612000284864

A randomised controlled crossover pilot study of meropenem standard 30 minute infusion versus prolonged 3 hour infusion in intensive care patients

A study of intensive care patients comparing meropenem 500mg 3 hour infusion versus 1g 30 minute infusion and time above mean inhibitory concentration


Sponsor

Austin Hospital

Enrollment

10 participants

Start Date

May 16, 2009

Study Type

Interventional

Conditions

Summary

Meropenem is an antibiotic used in the treatment of serious infections. This study aims to investigate whether giving meropenem a by a longer infusion (3 hours) but a lower dose, enables the antibiotic to be in the bloodstream for at least the same amount of time as a higher dose given over a short time (30 minutes).


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 100 Yearss

Inclusion Criteria3

  • Adult intensive care patients
  • Sepsis
  • Predicted duration of treatment more than 3 days

Exclusion Criteria2

  • Predicted duration of treatment < 3 days
  • Hypersensitivity to meropenem or other beta-lactams

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Interventions

Meropenem 500mg administered as a 3 hour infusion. Wash-out period between treatments of at least 24 hours.

Meropenem 500mg administered as a 3 hour infusion. Wash-out period between treatments of at least 24 hours.


Locations(1)

Australia

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