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临床试验/ACTRN12614001033639
ACTRN12614001033639终止4 期

The effect of different concentrations of bupivacaine and levobupivacaine on labour pain for primiparas, using patient-controlled epidural analgesia: Randomized controlled trial

Kestutis Rimaitis0 个研究点目标入组 504 人开始时间: 2014年9月25日最近更新:
适应症

试验速览

阶段
4 期
状态
终止
发起方
入组人数
504

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 40 Years(—)
性别
Female

入选标准

  • Primiparas, gestational age >37 and <41 weeks, who had requested for epidural analgesia during labor, cervical dilatation <5 cm, the beginning of labor is spontaneous. American Society of Anaesthesiologists (ASA) physical status 1 or 2;
  • Uncomplicated, vertex-presenting, singleton pregnancy.

排除标准

  • Arterial hypertension, preeclampsia, eclampsia.
  • Diabetes mellitus (gestational, type 1 and type 2).
  • There are contraindications for epidural analgesia due to haemodynamic, infectious, allergic, neurological or hematological reasons.
  • Multiple pregnancy, multiparity, induced labour
  • Body Mass Index >40 kg/m2, height less than 150 cm.
  • Fetal growth restrictions or other fetal abnormalities.

研究者

发起方
Kestutis Rimaitis

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