PACTR201908521430230尚未招募未知
Progress of labour with hyoscine-n-butyl bromide: a randomized double-blind placebo-controlled study
Fagbohun0 个研究点目标入组 172 人开始时间: 2019年7月26日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 172
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
- 年龄范围
- 19 Year(s) 至 44 Year(s)(—)
- 性别
- Female
入选标准
- •Multiparous pregnant women aged 18-40 years, with singleton pregnancy in cephalic presentation, admitted in active phase (at cervical dilatation of 4 to 6 cm) of spontaneous labour at term (37 weeks – 41 weeks + 6 days gestation) whose rate of cervical dilatation is less than 1 cm per hour as assessed four hours into admission
排除标准
- •Grand multiparity
- •Multiple pregnancy
- •Previous uterine scar
- •Cervical dilation = 7 cm at admission
- •Cervical cerclage
- •Chronic or pregnancy induced medical conditions
- •Presence of any contraindication to vaginal delivery
- •Allergy to hyoscine-n-butyl bromide
- •History suggestive of, or previous diagnoses of glaucoma, myasthenia gravis, obstructive uropathy, asthma, cardiac, liver or renal disease, seizure disorder or psychiatric illness
- •Prolonged Prelabour rupture of the fetal membranes (rupture of fetal membrane with latency period greater than 24hrs)
- •Congenital fetal malformations
- •Intra uterine growth restriction (IUGR)
- •Cephalopelvic disproportion
- •Intrauterine fetal death (IUFD)
- •Non consenting patient
研究者
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