跳至主要内容
临床试验/CTRI/2024/12/078272
CTRI/2024/12/078272尚未招募不适用

Inthrathecal levobupivacaine vs bupivacaine for infraumbilical surgery:A randomized control trial

JSS Academy of Higher Education and Research1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年12月29日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
to compare the sensory and motor block of 0.5% hyperbaric levo bupivacaine and o.5% hperbaric bupivacaine

研究概览

简要总结

All the patients will be admitted before surgery and pre anesthetic evaluation will be done.

After obtaining informed consent patients of ASA I and II  either gender undergoing elective infra umbilical surgery in whom spinal anesthesia is indicated will be include in the study.

On the day of surgery .in the operation theater ASA monitoring device will be attached and baseline recordings will be recorded

With patient sitting position lumbar puncture performed at L2-l3 level or L3-L4 level and the study drug is injected intra thecally and asses sensory and motor block onset time ,total duration of sensory and motor block,duration of effective analgesia and anesthesia

Hypotension and bradycardia also will noted down and treated accordingly

The study will also asses side effects such as nausea and vomiting

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • age :18-60 yrs,either sex ,ASA 1 and 2,patients undergoing infraumbilical surgery under spinal anaesthesia.

排除标准

  • spinal anomalies,contraindications to spinal anaesthesia, ASA 3 and 4,deranged coagulation profile,local infection at the surgical site.

结局指标

主要结局

to compare the sensory and motor block of 0.5% hyperbaric levo bupivacaine and o.5% hperbaric bupivacaine

时间窗: From time of spinal anaesthesia and noted at 0 minutes,5 minutes till 330 minutes

次要结局

  • To asses the sensory & motor block onset time ,total duration,asses & compare the side effects of hyperbaric bupivacaine & levobupivacaine(From the time of spinal anesthesia & noted at 0 minutes,5 minutes till 330 minutes.Till the patient feel pain at incision site)

研究者

发起方
JSS Academy of Higher Education and Research
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Alif Al Mohammed M

JSS Academy of Higher Education

研究点 (1)

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