跳至主要内容
临床试验/NCT01633294
NCT01633294已完成2 期

Antibiotic Prophylaxis in Prelabor Rupture of Membranes at Term - a Randomized Controlled Trial

Hospital de Santa Maria, Portugal1 个研究点 分布在 1 个国家目标入组 161 人开始时间: 2008年10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
161
试验地点
1
主要终点
neonatal infection rate

研究概览

简要总结

The aims of this study are to determine whether antibiotics administered routinely in women presenting with premature rupture of membranes later than the 37+0 weeks of gestation can alter the rate of maternal and neonatal infection and to compare these rates between prompt (< 12 hour) and delayed (≥ 12 hour) induction in the group of patients not submitted to antibiotic prophylaxis.

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

性别
Female
接受健康志愿者

入选标准

  • term (≥ 37+0 weeks) singleton pregnancy
  • a vertex presentation
  • ruptured membranes for less than 12 hours
  • negative Group B Streptococcus (GBS) culture performed between 35 and 37 weeks

排除标准

  • active labor
  • absence of GBS culture or indication for GBS antibiotic prophylaxis (such as maternal GBS colonization between 35 and 37 weeks, GBS bacteriuria, prior infant with GBS sepsis)
  • contraindication to expectant management (such as fetal distress, meconium staining of the amniotic fluid or chorioamnionitis) or to vaginal delivery

研究组 & 干预措施

Antibiotic group

Active Comparator

women submitted to antibiotic prophylaxis

干预措施: Ampicillin + gentamicin (Drug)

结局指标

主要结局

neonatal infection rate

时间窗: participants will be followed for the duration of hospital stay, an expected average of 3 days

neonatal infection rate includes early onset sepsis, meningitis and pneumonia

maternal infection rate

时间窗: participants will be followed for the duration of hospital stay, an expected average of 3 days

maternal infection rate includes chorioamnionitis or puerperal endometritis

次要结局

  • comparison of the infection rates between prompt and delayed induction(participants will be followed for the duration of hospital stay, an expected average of 3 days)

研究者

发起方
Hospital de Santa Maria, Portugal
申办方类型
Other
责任方
Principal Investigator
主要研究者

Filipa Faria Vaz Passos

Principal investigator

Hospital de Santa Maria, Portugal

研究点 (1)

Loading locations...

相似试验