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临床试验/NCT01309152
NCT01309152已完成不适用

Peri-and Postoperative Subcutaneous Adipose Tissue Cefazolin Determination Using Microdialysis in Morbidly Obese and Non-obese Patients

St. Antonius Hospital2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2

研究概览

简要总结

The investigators hypothesize that cefazolin perfusion to subcutaneous adipose tissue is reduced in morbidly obese patients. The primary objective of this exploratory pilot study is therefore to investigate target site (subcutaneous adipose tissue) penetration of cefazolin in morbidly obese patients and non-obese patients. The investigators aim to examine whether and how cefazolin plasma concentrations are predictive of subcutaneous (target) cefazolin concentrations. Possible factors of influence on the distribution of cefazolin (tissue perfusion, body weight, distribution of adipose tissue, other) will be identified.

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
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Body Mass Index > 40 kg/m2
  • BMI between 20-25
  • undergoing laparoscopic gastric banding, or bypass surgery or sleeve gastrectomy (See population description for surgery type of the non-obese group)
  • 21-60 years old
  • American Society of Anaesthesiologists (ASA) physical status II to III

排除标准

  • pregnancy
  • breastfeeding
  • known allergy for cefazolin/nadroparin
  • known ejection fraction of < 35%
  • renal insufficiency

研究者

申办方类型
Other

研究点 (2)

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