跳至主要内容
临床试验/NCT00463736
NCT00463736终止不适用

Magnesium Sulfate Versus Placebo for Tocolysis in Preterm Premature Rupture of Membranes

Regional Obstetrical Consultants1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2007年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
4
试验地点
1
主要终点
hours of latency to delivery

研究概览

简要总结

Study compares the outcomes of women between 26 and 32 wks gestation with rupture of membranes. Women randomized to receive tocolysis with magnesium sulfate x 48 hrs or placebo of saline IV x 48 hrs. Antibiotics and antenatal steroids given to both groups.

详细描述

The majority of studies of the effectiveness of tocolysis with PPROM were in the 1980s prior to the commmon usage of antenatal steroids and prophylactic maternal antibiotics. In most studies, tocolysis was not attempted prior to the onset of labor in this group of women. The ACOG Practice Bulletin of June 1998 concedes that the recommendation of tocolysis to permit administration of steroids and maternal antibiotics is based primarily upon consensus, not consistent scientific evidence.

The purpose of this study, which will randomize 128 subjects to tocolysis or no tocolysis, is to prospectively assess whether short term (48 hr) tocolysis affords benefit to women and babies between 26 and 32 weeks gestation with PPROM.

Subjects will be enrolled at 1-2 high risk hospitals in Chattanooga and Knoxville. All English and Spanish speaking women 18-45 years with PPROM and cervical dilation <4 will be eligible. Women with suspected intrauterine infection, positive fetal lung maturity, or > 6 hours tocolysis at time of admission will be excluded.

Both groups of women will receive continuous fetal monitoring, antibiotics, and antenatal steroids (if not previously administered). Both groups will be evaluated every 2-4 hours for fetal and maternal well being. Both groups will receive IVF at 125cc/hr, and the treatment group will be loaded with 4 grams of magnesium sulfate and receive maintainence dose of 2 grams/hr x 48 hrs.

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
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • English or Spanish speaking
  • preterm premature rupture of membranes
  • 26 - 32.6 weeks gestation
  • cervical dilation </= 4 cm

排除标准

  • suspected intrauterine or intraamniotic infection
  • > 6 hours of tocolysis prior to admission
  • positive fetal lung maturity

研究组 & 干预措施

Magnesium sulfate

Active Comparator

x 48 hours IV

干预措施: Magnesium sulfate (Drug)

Normal saline

Placebo Comparator

x 48 hours IV

干预措施: Magnesium sulfate (Drug)

结局指标

主要结局

hours of latency to delivery

时间窗: 0 hours to > 168 hours

from start of study drug to delivery

次要结局

  • maternal postpartum length of stay(0 hours to > 168 hours)
  • neonatal ventilator days(0 to 28 days)
  • neonatal early onset infection(0 to 28 days)
  • maternal infection rates(0 hours to > 168 hours)
  • neonatal length of stay(0 to 28 days)

研究者

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

Lorrie Mason

Christian Briery MD

Regional Obstetrical Consultants

研究点 (1)

Loading locations...

相似试验