PACTR202206902932545已完成未知
DROTAVERINE HYDROCHLORIDE VERSUS HYOSCINE BUTYLBROMIDE IN REDUCING FIRST STAGE OF LABOUR AMONG NULLIPARAE : A RANDOMIZED CONTROLLED TRIA
nenna S Nweke0 个研究点目标入组 165 人开始时间: 2022年3月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 165
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
- •1.Nulliparae
- •2.Women who consented to participate in the study
- •3.Women with fetus in cephalic presentation
- •4.Singleton fetus with no evidence of maternal or fetal distress.
- •5.Women with no contraindication to vaginal delivery.
- •6.Term pregnancies with intact or ruptured membranes
- •7.Cervical dilatation of 4-5 cm only
- •8.Spontaneous or induced labour
- •9.Patients on epidural
排除标准
- •1 Women with abnormal fetal presentation.
- •2. Women in latent phase of labour.
- •3. Preterm / term premature rupture of membranes.
- •4. Antepartum haemorrhage.
- •5. Those who refused to consent.
- •6. Previous uterine scar or surgery.
- •7. Huge fibroid in pregnancy.
- •8. Multiple gestations.
- •9. Multiparous or grand multiparous patients.
- •10. Medical diseases in pregnancy such as severe preeclampsia/eclampsia and others.
- •11. History of cervical surgery.
- •12. Hypersensitivity to drotaverine hydrochloride.
- •13. Any contraindication to vaginal delivery
研究者
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