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临床试验/NCT02569866
NCT02569866已完成2 期

Antibiotics After Breast Reduction:Clinical Trial With Randomization

Federal University of São Paulo1 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2014年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
124
试验地点
1
主要终点
Surgical site infection in the postoperative of reduction mammaplasty.

研究概览

简要总结

This study was designed to determine the role of antibiotics reduction mammaplasty influence surgical site infections rates.

详细描述

Prevention of SSI is important due to its morbidity, longer hospital stays and higher costs. In many surgical procedures where the risk of infection is relatively low and the postoperative infection can be treated properly, the role of antibiotics is not clear.

Despite the lack of evidence from prospective randomized controlled trials of evaluation, the use of antibiotics in plastic surgery is widespread in order to offer the highest safety standards patients.

The breast reduction is defined as "clean surgery" with a lower infection rate to 3.4%. Thus, the antibiotic is not recommended. However, studies have shown a real rate of infection associated with procedures ranging from 4-36%.

Thus, this trial was designed to verify the role of antibiotics in reduction mammaplasty.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Breast hypertrophy
  • Body mass index between 19 to 30 kg/m2

排除标准

  • Patients undergoing a surgical procedure in the breast
  • Diagnosis of breast pathology
  • Childbirth or lactation less than a year
  • Uncontrolled comorbidities
  • Use of immunosuppressive drugs
  • Misuse of capsules supplied
  • Absence during the weekly follow-up

研究组 & 干预措施

Antibiotics Group

Active Comparator

Capsules containing cephalexin/500mg will be administrated to the subjects, 4 times daily, for seven days during the postoperative period of reduction mammaplasty.

干预措施: Cephalexin (Drug)

Placebo Group

Placebo Comparator

Capsules containing placebo/500mg will be administrated to the subjects, 4 times daily, for seven days during the postoperative period of reduction mammaplasty.

干预措施: Placebo (Drug)

结局指标

主要结局

Surgical site infection in the postoperative of reduction mammaplasty.

时间窗: 30 days postoperatively

After surgery, the patients will be followed for 30 days and surgical site infection rates will be observed in both groups, according to the CDC criteria.

次要结局

未报告次要终点

研究者

发起方
Federal University of São Paulo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Edgard da Silva Garcia

Edgard da Silva Garcia, Professor, Universidade do Vale do Sapucaí

Federal University of São Paulo

研究点 (1)

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