临床试验/NCT00752908

NCT00752908已完成不适用

Tissue Penetration of Antibiotics in Obesity

Washington University School of Medicine1 个研究点分布在 1 个国家目标入组 27 人开始时间: 2008年2月最近更新: 2019年9月9日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方: Washington University School of Medicine
入组人数: 27
试验地点: 1
主要终点: Cefoxitin Plasma Concentrations

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to evaluate cefoxitin pharmacokinetics in obese surgical patients.

研究设计

研究类型: Observational
观察模型: Case Control
时间视角: Prospective

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•BMI <25 and >40
•Scheduled for elective abdominal or pelvic surgery
•Surgical plan for intraoperative cefoxitin prophylaxis
•Able to provide informed consent

排除标准

•Allergy to Cefoxitin
•Renal or Hepatic insufficiency

结局指标

主要结局

Cefoxitin Plasma Concentrations

时间窗: 8 hours

Cefoxitin plasma concentrations

次要结局

Cefoxitin Tissue Concentrations(8 hours)

研究者

发起方

Washington University School of Medicine

申办方类型

Other

责任方

Sponsor

研究点 (1)

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