Status:

UNKNOWN

Plasma and Lung Tissue Concentrations of Linezolid in Septic Shock Patients

Lead Sponsor:

Southeast University, China

Collaborating Sponsors:

Cttq

Conditions:

Septic Shock

Eligibility:

All Genders

19-75 years

Brief Summary

The study measures the plasma and bronchoalveolar lavage fluid concentrations of linezolid in septic shock patients comparing with non-septic shock patients to confirm the impact of septic shock on PK...

Detailed Description

A wide array of pathophysiological changes occurring in severe sepsis and septic shock patients may influence antibiotics' pharmacokinetic (PK) properties. The pharmacokinetics and tissue distribution...

Eligibility Criteria

Inclusion

  • between 18 years old and 75 years old;
  • Admitted to the ICU;
  • Expectation, in the opinion of the investigator, that the patients' infection will require ICU stay more than 3 days;
  • Patients diagnosed as severe pneumonia requiring mechanical ventilatory support;
  • Severe pneumonia known or suspected to be caused by Gram-positive pathogens;
  • Expected to treat with linezolid.

Exclusion

  • Unable to take bronchoalveolar lavage via bronchofiberscopy;
  • Allergy, hypersensitivity or a serious reaction to linezolid;
  • Treatment with linezolid during the previous 72 hours;
  • Pregnancy.

Key Trial Info

Start Date :

October 20 2017

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

April 30 2018

Estimated Enrollment :

46 Patients enrolled

Trial Details

Trial ID

NCT03308227

Start Date

October 20 2017

End Date

April 30 2018

Last Update

October 12 2017

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