跳至主要内容
临床试验/PER-033-05
PER-033-05未知未知

INEZOLID AGAINST VANCOMYCIN / CEFAZOLINE IN THE TREATMENT OF PATIENTS SUBJECTED TO HEMODIALYSIS WITH BLOODSTREAM INFECTIONS RELATED TO CATHETERS AND CAUSED BY GRAM-POSITIVE MICRORGANISMS

PFIZER S.A.,0 个研究点目标入组 0 人开始时间: 2005年7月1日最近更新:
适应症

试验速览

阶段
未知
发起方
PFIZER S.A.,

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Male or female 18 years of age or older and with a body weight> 40 Kg.
  • 2. Patients with end-stage renal disease undergoing hemodialysis, with the following: A) Signs and symptoms of a localized infection related to catheters. B) A body temperature> 38.0 ° C or <36 ° C. C) A positive blood culture for Gram-positive microorganisms.
  • 3. Presence of at least one of the following systemic signs of infection: A) Hypotension. B) Tachycardia. C) Tachypnea. D) Leukocyte count> 10,000 cells / mm3 or <4,000 cells / mm3, or with a differential count showing> 10% abasted neutrophils.
  • 4. Patients undergoing hemodialysis with tunneled or non-tunneled catheters.
  • 5. Patients who are willing and able to comply with scheduled visits, plan for treatment, laboratory tests and other study procedures.

排除标准

  • 1. Bloodstream infections related to catheters caused by Gram-negative bacteria, fungi, mixed cultures of Gram-negative bacteria and Gram-positive bacteria or mixed cultures with Gram positive / negative bacteria and fungi.
  • 2. Patients with evidence of other infections that result in bacteremia.
  • 3. Patients in whom the infected catheter can not be removed.
  • 4. Patients with permanent intravascular devices.
  • 5. Women with potential to have family who are not able or who do not wish to take adequate contraceptive precautions, who have a positive result in a test to diagnose the pregnancy within 24 hours before entering the study, that is known are pregnant, or are currently breastfeeding an infant.
  • 6. Identification of a pathogen resistant to linezolid or vancomycin.
  • 7. Patients who are unlikely to survive throughout the treatment and evaluation periods.
  • 8. Administration of a glycopeptide antibiotic within 5 days before enrollment.
  • 9. Previous enrollment in the present protocol.
  • 10. Hypersensitivity to linezolid, vancomycin, gentamicin or to any of its excipients.
  • 11. Concurrent use of another medication in research or use within 30 days of entering the study.
  • 12. Patients with hemodynamic compromise resistant to pressors and fluids, or with pulmonary embolism.

研究者

发起方
PFIZER S.A.,

相似试验