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临床试验/NCT01169064
NCT01169064终止不适用

Topical Silver for Prevention of Wound Infection Post Cesarean Delivery: A Randomized Controlled Trial

Vanderbilt University2 个研究点 分布在 1 个国家目标入组 475 人开始时间: 2010年7月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
475
试验地点
2
主要终点
Silver Treatment Efficacy

研究概览

简要总结

A common concern in any surgical procedure is the occurrence of infection. Silver-containing treatments are popular and used in wound treatment; however, there is presently little evidence of the effectiveness of silver-containing treatment for the prevention of obstetrical wound infection. We plan to investigate the rate of infection in women experiencing cesarean sections at Vanderbilt University Medical Center (VUMC) by comparing the infection rate based on a randomized choice of silver-containing wound dressings to soft cloth adhesive wound dressings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Cesarean delivery with pfannenstiel incision

排除标准

  • Incision other than pfannenstiel
  • Silver allergy
  • Inability to provide informed consent

结局指标

主要结局

Silver Treatment Efficacy

时间窗: 6 weeks postpartum

As measured by number of patients with postop infections at 6 wks

次要结局

  • Infection Rate Adjusted for Maternal BMI(6 weeks postpartum)
  • Patient Dressing Cost(Postoperative)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kelly Bennett

Associate Professor

Vanderbilt University

研究点 (2)

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