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临床试验/NCT03246360
NCT03246360
已完成
不适用

Pharmacological Comparison of Continuous and Intermittent Infusions of Cloxacillin During Bone and Joint Infections: a Prospective, Randomized, Open-label, Monocentric Crossover Study.

Centre Hospitalier Universitaire de Nice1 个研究点 分布在 1 个国家目标入组 12 人2017年11月23日

概览

阶段
不适用
干预措施
Modification for administration mode of cloxacillin antibiotic
疾病 / 适应症
Infection
发起方
Centre Hospitalier Universitaire de Nice
入组人数
12
试验地点
1
主要终点
The equivalence of the Pharmacokinetic-Pharmacodynamic indicators commonly used for the study of betalactamines: T> minimal inhibitory concentration
状态
已完成
最后更新
上个月

概览

简要总结

Our objective is to establish pharmacological equivalence of intermittent and continuous infusion of cloxacillin during methicillin-susceptible Staphylococcus aureus (MSSA) bone and joint infections (BJI). Twelve patients suffering MSSA BJI will receive both administration modalities and serum concentrations of cloxacillin will be determined after 3 days of II and 3 days of continuous infusion in a prospective, randomized, open-label, monocentric crossover study design.

详细描述

Introduction Staphylococcus aureus is the main causative agent of bone and joint infections (BJI). More than 80% of the strains isolated in France are methicillin-susceptible (MSSA). During the early phase of MSSA BJI management national and international guidelines recommend the use of intra-venous type M penicillin with a dosage ranging from 100 to 200 mg/kg/day. Pharmacological properties of this class of penicillin require 4 to 6 infusions by day. Continuous infusion of beta-lactams is increasingly used especially in intensive care units. It allows an improvement of pharmacokinetic/pharmacodynamics (PK/PD) parameters and a reduction in time dedicated to infusion preparations by the nurses. However pharmacological data regarding such administration is required for type M penicillin. Design A 6-day, prospective, randomized, open-label, monocentric crossover study Participants Twelve adult patients with MSSA BJI Intervention Patients will be randomized in two groups: the first group will receive 3 days of cloxacillin (150 mg/kg/day) through 4 intermittent infusions/day followed by 3 days of cloxacillin (150 mg/kg/day) through continuous infusion (2 infusions during 12 hours). In the second group the infusion modalities will be inverted and continuous infusion will be preceded by a loading dose. Serum concentrations of cloxacillin will be determined at Day 3 and Days 6 The area under the curve / minimal inhibitory concentration ratio will be use to establish the equivalence between both administration modalities.

注册库
clinicaltrials.gov
开始日期
2017年11月23日
结束日期
2018年9月18日
最后更新
上个月
研究类型
Interventional
研究设计
Crossover
性别
All

研究者

入排标准

入选标准

  • Staphylococcus aureus sensitive to methicillin and to be treated with cloxacillin by injectable antibiotic monotherapy For patients with Osteo-articular infection on material
  • Presence of a fistula in contact with the prosthesis or implant.
  • Pus in the joint or in contact with the prosthesis or implant
  • Presence of at least 1 positive sample (1 sampling by articular puncture or 1 peroperative sampling or by blood culture)
  • A histological analysis of the peri-prosthetic osteo-articular tissue which is the object of acute inflammation is a strong argument in favor of an Osteo-articular infection on material
  • For spondylodiscitis
  • Culture of a disco-vertebral biopsy puncture to isolate a methicillin sensitive S. aureus
  • Positive haemocultures for S. aureus sensitive to methicillin with imaging examination (CT or MRI of the spine) showing images of spondylodiscitis
  • For primitive arthritis :
  • Culture of a positive methicillin-sensitive S. aureus articular fluid puncture

排除标准

  • Allergy to betalactamines
  • Taking penicillin M within 36 hours before inclusion Renal function impaired with a glomerular filtration rate measured by MDRD formula of less than 30 ml / min
  • Patient with renal function expected to change within 6 days of inclusion
  • Hepatocellular insufficiency, whatever the degree
  • \*Methotrexate intake
  • Polytransfused (more than 2 CGR) in the previous week
  • Patients requiring resuscitation

研究组 & 干预措施

Intermittent administration of cloxacillin

干预措施: Modification for administration mode of cloxacillin antibiotic

continuous administration of cloxacillin

干预措施: Modification for administration mode of cloxacillin antibiotic

结局指标

主要结局

The equivalence of the Pharmacokinetic-Pharmacodynamic indicators commonly used for the study of betalactamines: T> minimal inhibitory concentration

时间窗: Six days

The equivalence of the Pharmacokinetic-Pharmacodynamic indicators commonly used for the study of betalactamines: the area under the curve (AUC) / minimal inhibitory concentration

时间窗: Six days

研究点 (1)

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