drugset / Trial / NCT03452839

Bolus Versus Continuous Infusion of Meropenem

NCT03452839

Phase 4 Completed 607 enrolled Vita-Salute San Raffaele University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study arises from the need to optimize antibacterial drug usage to face increasing drug resistance among gram-negative pathogens in intensive care units. Gram-negative organisms are responsible for 70% of drug-resistant infections acquired in the intensive care unit. Meropenem is a β-lactam, carbapenem, antibacterial agent usually administered by intermittent infusion. As β-lactam efficacy is determined by the time in which the drug concentration exceeds the minimum inhibiting concentration of the target pathogen, intermittent infusion of this short half-lived drug can lead to precipitous drops in serum drug levels, an occurrence linked to emergence of resistant pathogens. The investigators hypothesize a beneficial effect of a continuous meropenem infusion on mortality and emergence of drug resistant pathogens. All patients enrolled will receive 1 g of meropenem bolus. After that, subjects will be randomized to receive a continuous infusion of study drug 3g/day or a bolus administration of the same amount of drugs. The investigators expect a reduction of mortality and emergence of extensive or pan drug resistant pathogens from 52 to 40% in the continuous infusion group.

Timeline

Start
2018-06-05
Primary completion
2022-10-01
Completion
2022-12-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Meropenem Small molecule 1 g
Subject Meropenem Small molecule 2 g
Subject Meropenem Small molecule 3 g

Indications