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临床试验/CTRI/2025/01/079554
CTRI/2025/01/079554尚未招募4 期

Comparison Of Levo-Bupivacaine Fentanyl and Levo-Bupivacaine Fentanyl with Magnesium Sulphate as Adjuvants to Spinal Anaesthesia in Infra-umblical Surgeries

Keerthana J1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年2月17日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
To compare the duration of sensory block when intrathecal Magnesium sulphate is added with low doseLevo Bupivacaine Fentanyl Spinal Anesthesia with spinal Anesthesia given only with Levo bupivacaine & Fentanyl

研究概览

简要总结

This study is a Randomised double blinded control study in which the participants will equally be divided into 2 groups.

The person performing the procedure will be unrealated to the study and will be performing the spinal anesthesia technique with drugs given to him in sealed envelopes.

The principle investigator who will be blinded to the drug given will be noting the required paremeters in the post-operative period

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
20.00 Day(s) 至 60.00 Day(s)(—)
性别
All

入选标准

  • Age between 20years to 60 years All patients undergoing Infraumblical surgery.

排除标准

  • Patients not willing for spinal anesthesia Patients with severe cardiac diseases Patients with age less than 20 years and more than 60 years Patients with coagulopathies Patients with infections in the spine.

结局指标

主要结局

To compare the duration of sensory block when intrathecal Magnesium sulphate is added with low doseLevo Bupivacaine Fentanyl Spinal Anesthesia with spinal Anesthesia given only with Levo bupivacaine & Fentanyl

时间窗: VAS score will be assessed every 2 hours in the post operative period until it is less than 4

次要结局

  • To compare the onset of sensory and motor blockade in both the groups(every minute for first 5 minutes)

研究者

发起方
Keerthana J
申办方类型
Other [Self ]
责任方
Principal Investigator
主要研究者

Keerthana J

ACSMCH

研究点 (1)

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