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Evaluation of Patients With Methicillin-Resistant Staphylococcus Aureus Hospital-Acquired Pneumonia Treated With Linezolid or Vancomycin

Pfizer logo

Pfizer

Status

Completed

Conditions

Methicillin-Resistant Staphylococcus Aureus (MRSA)
Hospital-Acquired Pneumonia

Treatments

Drug: Linezolid
Drug: Vancomycin

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01561469
A5951168

Details and patient eligibility

About

The objective of this study is to review the local management of patients with methicillin-resistant Staphylococcus aureus hospital-acquired pneumonia treated with vancomycin or linezolid with the goal to define if any difference exists among these antimicrobials in regard to clinical and economic outcomes.

Full description

Non-randomized, retrospective, observational study

Enrollment

188 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients will be enrolled in the study if they fulfill the following three inclusion criteria:

  1. Protocol criteria for HAP/VAP: Criteria for making a correct diagnosis of HAP will be met if the patient develops a new or progressive pulmonary infiltrate associated with at least two of the following: new or increased respiratory symptomatology (cough, sputum or tracheal secretions, shortness of breath), fever or hypothermia, leukocytosis, left shift, or leukopenia, or deterioration of pulmonary function.
  2. Isolation of MRSA from a respiratory sample or blood culture within 48 hours of the diagnosis of HAP/VAP
  3. Treatment of MRSA HAP/VAP with either vancomycin or linezolid with incorporation of 100 patients in the vancomycin arm and 100 patients in the linezolid arm

Exclusion criteria

Patients not meeting enrollment criteria.

Trial design

188 participants in 2 patient groups

Linezolid observational cohort
Treatment:
Drug: Linezolid
Vancomycin observational cohort
Treatment:
Drug: Vancomycin

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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