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临床试验/NCT00599898
NCT00599898已完成4 期

Nifedipine Compared to Atosiban for Treating Preterm Labor. A Randomized Controlled Trial.

Raed Salim1 个研究点 分布在 1 个国家目标入组 145 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
145
试验地点
1
主要终点
delaying labor

研究概览

简要总结

The purpose of this study is to investigate the efficacy and the safety of nifedipine compared to atosiban for treating preterm labor.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Gestational age between 24 to 34 weeks which had been documented by a definite LMP and sonography up to 20 weeks.
  • All women fulfilled the criteria of preterm labor. The diagnosis of preterm labor required the presence of 4 uterine contractions or more over 30 minutes, each lasting at least 30 seconds, and documented cervical change. The cervical criteria were met when either of the following was present:
  • Nulliparous women: a single cervical examination demonstrating dilatation of 0 cm to 4 cm and effacement of at least 50%
  • Multiparous women: a single cervical examination demonstrating dilatation of 1 cm to 4 cm and effacement of at least 50%.
  • Provision of written informed consent

排除标准

  • Chorioamnionitis
  • Preterm rupture of membranes
  • Vaginal bleeding
  • Major fetal malformations
  • Severe hypertensive disorders
  • Intrauterine growth restriction (< 5th percentile).
  • Non-reassuring fetal heart rate
  • Maternal contraindications
  • Chronic hypertension
  • Systolic blood pressure < 90 mmHg
  • Cardiovascular disease
  • Elevated hepatic enzymes
  • Congenital or acquired uterine malformation

研究组 & 干预措施

1

Experimental

干预措施: Atosiban (Drug)

2

Experimental

干预措施: Nifedipine (Drug)

结局指标

主要结局

delaying labor

时间窗: for more than 48 hours after starting treatment

次要结局

  • drugs side effects(within the first 48 hours after treatment)
  • obstetrical (number of days to delivery, gestational age at delivery, mode of delivery)(within 24 hours after delivery)
  • neonatal (Apgar score, sepsis, IVH, NEC, RDS, DEATH)(within 30 days from delivery)

研究者

发起方
Raed Salim
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Raed Salim

MD

HaEmek Medical Center, Israel

研究点 (1)

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