跳至主要内容
临床试验/CTRI/2017/11/010545
CTRI/2017/11/010545招募中不适用

A study to test the efficacy and safety of pre-procedure ultrasound guided paramedian technique as compared to conventional landmark guided median technique in administering spinal anesthesia

Armed Forces Medical College1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2016年5月12日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
74
试验地点
1
主要终点
Total number of needle passes

研究概览

简要总结

A study to compare safety and efficacy of pre-procedure ultrasound guided paramedian technique as compared to landmark guided median technique for administering spinal anesthesia

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
50.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • age 50 years and above consented patients scheduled for elective lower abdominal ,pelvic , lower limb surgeries.

排除标准

  • below 50 yrs contraindication to spinal anesthesiaallergy to local anesthetic coagulopathy local site infection indeterminate neurologic disease.

结局指标

主要结局

Total number of needle passes

时间窗: 0

Total number of needle insertion attempts

时间窗: 0

次要结局

  • Incidence of radicular pain,paresthesia(Incidence of blood in spinal needle)

研究者

申办方类型
Government medical college

研究点 (1)

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