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
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
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