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临床试验/NCT03306290
NCT03306290已完成不适用

An Evaluation of Serum Concentration of CEFOxitin Used for Antibiotic Prophylaxis in Severely and Morbidly Obese Patients Undergoing BARiatric Surgery (CEFOBAR)

Central Hospital, Nancy, France1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2017年10月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200
试验地点
1
主要终点
Serum concentration of Cefoxitin at the beginning and end of the surgery with one extra measurement at halfway surgery

研究概览

简要总结

Obesity is a pandemic problem in modern societies. Bariatric surgery (gastric by-pass and sleeve gastrectomy) has emerged as an efficient treatment to reduce morbidity and mortality related to obesity. Obesity and bariatric surgery are known to be risk factors of surgical site infections (SSI). The occurrence of SSI increases health cost and the duration of hospitalization. However, an appropriate antibiotic prophylaxis has been shown to reduce SSI. As recommended by several national societies, the antibiotic prophylaxis dose should be increased in the severely obese population. However, this recommendation lies on a low level of evidence. Besides, great disparities regarding obese patient antibiotic prophylaxis exist between countries and adequate doses are still not clearly defined. In France, for instance, the intravenous second generation cephalosporin CEFOXITIN is used for antibiotic prophylaxis in bariatric surgery at the initial loading dose of 4g (2-fold that of non-obese population) at the beginning of surgery.

Obese patients have increased risk of under-dosage due to modification of their pharmacokinetics (fat/lean mass, distribution volume, renal clearance, etc.). Only few studies, all investigating a low amount of patients, evaluated the appropriateness of intraoperative antibiotic prophylaxis dosage of different betalactam and cephalosporin in the obese population. This population was more likely to be under-dosed.

The aim of this study is to analyse the appropriateness of the reference dose of intravenous Cefoxitin used as antibiotic prophylaxis in severely obese patients undergoing bariatric surgery. This will be a 2-year prospective monocentric study held in the University Hospital of Nancy, France. A large group of obese patients (~300) will be included. Serial serum concentration measurements of Cefoxitin will be performed before, during, and at skin closure of the bariatric surgery. This study will give insights in pharmacokinetics of the antibiotic prophylaxis in the obese population and will help to determine the initial dosage and the optimal method for antibiotic prophylaxis administration.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Age ≥ 18 years-old,
  • Severely obese patient with a BMI ≥ 35 kg.m-2,
  • Scheduled bariatric surgery: gastric by-pass or sleeve gastrectomy,
  • Affiliated to social security,
  • The patient is able to consent to clinical research and has received all information on the study design/protocol,
  • Signed/written informed consent

排除标准

  • Refuse to consent to the study or the patient is unable to consent,
  • Allergy/Anaphylaxis to beta-lactam (ß-lactam) antibiotics either proven or suspected,
  • Pregnancy,
  • Persons deprived of their liberty by judicial or administrative decision,
  • Urgent or emergent surgery.

研究组 & 干预措施

Bariatric surgery candidate

Other

Patients included in this study belong to this arm and put up with intervention "Serum dosage of antibiotic prophylaxis CEFOXITIN"

干预措施: Serum dosage of antibiotic prophylaxis CEFOXITIN (Drug)

结局指标

主要结局

Serum concentration of Cefoxitin at the beginning and end of the surgery with one extra measurement at halfway surgery

时间窗: baseline

Blood samples will be put at low temperature for transportation and then analysed by chromatographic method

次要结局

  • Pharmacokinetic parameters: drug clearance(baseline)
  • Pharmacokinetic parameter: volume of distribution(baseline)
  • Pharmacokinetic parameter: half-life(baseline)
  • Pharmacokinetic parameter: elimination rate(baseline)
  • Incidence of deep incisional surgical site infection (SSI) at 30 days(up to 30 days after surgery)
  • Identification of factors that may be associated with the risk of under-dosage(baseline)
  • Pharmacokinetic parameter: area under curve,(baseline)
  • Incidence of superficial incisional surgical site infection (SSI) at 30 days(up to 30 days after surgery)
  • Incidence of organ/space surgical site infection (SSI) at 30 days(up to 30 days after surgery)

研究者

发起方
Central Hospital, Nancy, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

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