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临床试验/ACTRN12614000893606
ACTRN12614000893606尚未招募未知

Transient hip and knee flexion for rapid onset spinal anaesthesia (ROSA) for women undergoing elective caesarean section, a randomised control study to evaluate the time from completing spinal injection until the anaesthetist determines surgery can proceed and surgery commences.

Dr. Allan Cyna0 个研究点目标入组 40 人开始时间: 2014年8月22日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
40

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
Open (masking not used)

入排标准

年龄范围
18 Years 至 50 Years(—)
性别
Female

入选标准

  • Parturients having elective lower segment caesarean section under spinal anaesthesia

排除标准

  • Women <18 years old
  • Women requiring an interpreter when one is unavailable
  • Women with an intellectual or mental impairment
  • Women with pre-existing medical, rheumatologic or orthopaedic conditions which prevents them from performing the manoeuvre correctly e.g. recent lower limb fracture, ankylosing spondylitis.

研究者

发起方
Dr. Allan Cyna

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