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临床试验/CTRI/2023/08/056421
CTRI/2023/08/056421尚未招募1/2 期

Efficacy of intrathecal 0.5% Bupivacaine with fentanyl & 0.5% Bupivacaine with Butorphanol in lower limb surgeries

DR Ramachandran R1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年8月26日最近更新:

试验速览

阶段
1/2 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
and 0.5% Bupivacaine with butorphanol

研究概览

简要总结

The main aim of the study is to compare the efficacy of intrathecal 0.5% Bupivacaine with Fentanyl and Burophanol using spinal anaesthesia.

研究设计

研究类型
Interventional
分配方式
Stratified block randomization
盲法
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

  • Patient Posted for lower limb surgical and orthopaedic procedures Patient who are accepted under ASA PS1 and ASA PS2.

排除标准

  • Patient who refused to give consent for study Patient who are haemodynamically unstable.

结局指标

主要结局

and 0.5% Bupivacaine with butorphanol

时间窗: Motor & sensory blockade checked every 15 mins

duration of motor & sensory blockade between 0.5% bupivacaine with Fentanyl

时间窗: Motor & sensory blockade checked every 15 mins

次要结局

  • haemodynamic parameters between two drugs

研究者

发起方
DR Ramachandran R
申办方类型
Private medical college

研究点 (1)

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