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Monitoring of Piperacillin-Tazobactam and Meropenem Plasmatic Levels in Critical Patients

F

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Status

Unknown

Conditions

Septic Shock
Sepsis

Treatments

Drug: Piperacillin/tazobactam or Meropenem

Study type

Observational

Funder types

Other

Identifiers

NCT04257838
FIS-MER-2019-01

Details and patient eligibility

About

The aim of this study is to establish the Piperacillin-Tazobactam and Meropenem Plasmatic Levels to know if it´s necessary to make some adjustment in the recommended dose regimen.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients above 18 years old.
  • Hospitalized in the Intense Care Unit.
  • Patients treated with Piperacillin-Tazobactam or Meropenem.
  • Septic shock.
  • Renal hyper clearance.
  • Gram-negative bacillary bacteremia.
  • Continuous renal replacement technique.
  • ECMO.
  • Obesity (BMI> 40).

Exclusion criteria

  • Patients under 18 years old.
  • Pregnant women.

Trial design

200 participants in 1 patient group

Piperacillin-Tazobactam or Meropenem Cohort
Description:
Patients hospitalized for sepsis or septic shock that are treated with Piperacillin-Tazobactam or Meropenem and meet all the inclusion criteria and none of the exclusion criteria.
Treatment:
Drug: Piperacillin/tazobactam or Meropenem

Trial contacts and locations

1

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Central trial contact

Marta María Pinilla de Torre

Data sourced from clinicaltrials.gov

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