跳至主要内容
临床试验/NCT01852188
NCT01852188已完成不适用

A Comparison of Sterile and Non-sterile Gloves for the Incidence of Chorioamnionitis During Labor: a Randomized Controlled Trial

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 507 人开始时间: 2011年5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
507
试验地点
2
主要终点
Clinical chorioamnionitis

研究概览

简要总结

The purpose of this study is to determine whether the use of sterile or clean gloves during labor exams affects the rate of chorioamnionitis. Chorioamnionitis is an infection of the membranes around the baby.

详细描述

The importance of this study is that intrapartum vaginal exams (while patients are laboring) are performed routinely in modern obstetrical practice, and there is no randomized trial available assessing the relationship between the type of glove used and the rate of chorioamnionitis.

研究设计

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

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

  • Spontaneous or induced labor
  • Rupture of membranes < 12 hours
  • Nulliparous or multiparous
  • Gestational age greater than or equal to 34 weeks
  • Age greater than or equal to 18

排除标准

  • Contraindications to labor
  • Multiple gestations
  • Rupture of Membranes greater than 12 hours
  • Gestational age less than 34 weeks
  • Non-English speaking patients

研究组 & 干预措施

Nonsterile

Other

Patients will be randomized to either sterile or clean gloves during intrapartum vaginal exams.

干预措施: Type of glove used for intrapartum vaginal exams (Other)

Sterile

Other

Patients will be randomized to either sterile or clean gloves during intrapartum vaginal exams.

干预措施: Type of glove used for intrapartum vaginal exams (Other)

结局指标

主要结局

Clinical chorioamnionitis

时间窗: participants will be followed during their intrapartum hospital stay, an expected average of 48-72hrs

Clinical chorioamnionitis with at least two of the four criteria met-maternal fever of 38 degrees Celsius or greater, maternal tachycardia (pulse \>100), fetal tachycardia (fetal heart rate \>160), and/or fundal tenderness

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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