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临床试验/CTRI/2020/09/027861
CTRI/2020/09/027861尚未招募未知

FINDING THE OPTIMAL CONCENTRATION OF ROPIVACAINE FOR LABOUR PAIN MANAGEMENT USING PARTURIENT CONTROLLED EPIDURAL ANALGESIA (PCEA): A DOUBLE BLIND, RANDOMIZED TRIA

maid Hospital Dr SNMedical College Jodhpur0 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
未知
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

  • healthy primi gravida women with a
  • singleton fetus in cephalic presentation at term (>= 37 weeksâ?? gestation), who will request
  • epidural analgesia; an American Society of Anesthesiologists (ASA) physical status class 2; no
  • contraindications for epidural analgesia.

排除标准

  • BMI more than 35 kg/m2 ; gestational diabetes; hypertensive disorders; induced labor; premature
  • rupture of membranes ( >18 h duration); fetal growth retardation or a fetus with physical
  • abnormalities. Patients will be excluded from the study if any complications develop that
  • requires cessation of the epidural infusion. This includes patients who have ineffective
  • analgesia, in whom there will be a need to change LA concentration or study design.

研究者

发起方
maid Hospital Dr SNMedical College Jodhpur

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