跳至主要内容
临床试验/NCT00844636
NCT00844636已完成不适用

A Randomized Trial of Blunt Needles for the Reduction of Needlestick Injuries During Cesarean Section

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2005年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
194
试验地点
2
主要终点
Number of observed glove perforations

研究概览

简要总结

The objective of this study was to determine if blunt needle use during cesarean section closure protects against glove perforation and percutaneous injury to the surgeon and surgical assistant. A secondary objective was to determine physician satisfaction with blunt needles during the surgery.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Undergoing a cesarean section

排除标准

  • Under age 18
  • Non-English speaking

研究组 & 干预措施

Sharp Needles

Active Comparator

Sharp needles to close uterus, fascia and skin during cesarean section

干预措施: Sharp needle (Device)

Blunt Needles

Active Comparator

Assignment to blunt needles to close uterus, fascia and skin during cesarean section

干预措施: Blunt needles (Device)

结局指标

主要结局

Number of observed glove perforations

时间窗: 1 day

review post-op

次要结局

  • Physician satisfaction with the needle assignment(1 day)

研究者

申办方类型
Other

研究点 (2)

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