CTRI/2018/08/015161尚未招募4 期
Study of efficacy and safety of Intravenous Paracetamol Infusion as intrapartum analgesic: Randomized Control Trial
CRH Sikkim Manipal Institute of Medical Sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
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
入选标准
- •1.Age between 18-35 years.
- •2.Primigravida and multigravida
- •3.The gestational age between 37- 42 weeks.
- •4.Patient seeking analgesia.
- •5.Single viable fetus.
- •6.Vertex presentation.
- •7.1st stage of labour with cervical dilatation 3-4 cm (in active phase).
排除标准
- •1.Extreme of age (below 18-above 35).
- •2.Multiple gestation.
- •3.Malpresentation.
- •4.Major degree of cephalopelvic disproportion.
- •5.Any medical disorder with pregnancy e.g., Rheumatic heart disease, Diabetes mellitus, Hypertension.
- •6.Use of any other kind of analgesia before recruitment in the study
- •7.Scared uterus.
- •8.Fetal distress.
- •9.Antepartum hemorrhage.
- •10.Polyhydramnios.
- •11.Intra uterine infections.
- •12.Hypersensitivity to paracetamol.
研究者
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