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临床试验/CTRI/2018/02/011711
CTRI/2018/02/011711已完成4 期

A randomised control trial comparing intrathecal ropivacaine, levobupivacaine and bupivacaine for caesarean section

ESICPostgraduate Institute of Medical Sciences and Research0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
100

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

  • Full term patients scheduled for caesarean section of ASA status1 and 2, age group of 18 to 40 years, body weight of 45 to 85 kg and height of 145 to165cm.

排除标准

  • Parturients with hypersensitivity to local anesthetics, contraindications to neuraxial block, twin pregnancy, obstetric complications or fetal compromise were excluded

研究者

发起方
ESICPostgraduate Institute of Medical Sciences and Research

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