跳至主要内容
临床试验/CTRI/2024/05/066935
CTRI/2024/05/066935尚未招募不适用

A Randomised comparative study between hyperbaric Levobupivacaine(0.5%) and hyperbaric Ropivacaine(0.75%) in lower limb surgeries under spinal Anaesthesia.

LLRM Medical College1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年5月20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
80
试验地点
1
主要终点
The primary outcome is to study the efficacy of the drug based on Duration of motor blockade , assessed by Modified Bromage scale.

研究概览

简要总结

This study will be carried out to compare the efficacy of Hyperbaric Levobupivacaine and Hyperbaric Ropivacaine in patients undergoing lower limb Surgeries under Spinal Anaesthesia.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • ASA GRADE I and II Age between 18 to 65 years Patients undergoing lower limb Surgeries.

排除标准

  • Patient Refusal Infection at the Injection Site Coagulopathy Increased Intracranial Pressure Known Allergy or Hypersensitivity to Local Anaesthetic Agents.

结局指标

主要结局

The primary outcome is to study the efficacy of the drug based on Duration of motor blockade , assessed by Modified Bromage scale.

时间窗: Baseline vitals will be noted. After Spinal anesthesia, Haemodynamic parameters ( SBP,DBP,MAP,HR), Loss of sensory and motor function will be noted every 1 minute for first 5 minutes, every 2 minutes for next 10 minutes, every 5 minutes for next 25 minutes and then every 30 minutes till regression of block.

次要结局

  • 1.To compare and Evaluate Onset of sensory block in both the groups(2.To compare and Evaluate Onset of motor block in both the groups)

研究者

发起方
LLRM Medical College
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Vaibhav Tiwary

Llrm medical college

研究点 (1)

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