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临床试验/ISRCTN20129681
ISRCTN20129681已完成不适用

Transdermal nitroglycerin to reduce the incidence of neonatal mortality in women who present in preterm labour: a placebo-controlled randomised trial

Queen's University (Canada)0 个研究点目标入组 600 人开始时间: 2005年9月26日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Greater than or equal to 24 to less than or equal to 32 weeks gestational age based on menstrual dates or earliest ultrasound scan
  • 2. Preterm labour:
  • 2.1. At least four painful uterine contractions per 20 minutes
  • 2.2. Change in the cervix (change in bishop score or bishop score greater than or equal to 6)

排除标准

  • 1. Any maternal (e.g. significant antepartum haemorrhage) or foetal (e.g. non-reassuring heart rate pattern) condition necessitating immediate delivery
  • 2. Multiple gestations (i.e. twins, triplets etc.)
  • 3. Premature prelabour rupture of the membranes (PPROM)
  • 4. Intrauterine foetal demise or lethal foetal anomalies
  • 5. Cervix dilated greater than 8 cm
  • 6. Treatment with another agent within 24 hours
  • 7. Previous enrolment in this trial
  • 8. Known sensitivity to GTN
  • 9. Failure to give consent

研究者

发起方
Queen's University (Canada)

相似试验

The Canadian preterm labour nitroglycerin trial | 临床试验