跳至主要内容
临床试验/CTRI/2025/02/081405
CTRI/2025/02/081405尚未招募不适用

Dose response of perineural magnesium sulphate in ultrasound guided infraclavicular brachial plexus block– A randomized double-blind study

Dr Arun Parthasarathy1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年4月10日

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
Proportion of participants with at least 150 minutes increase in the duration of analgesia when compared to the other groups.

研究概览

简要总结

Regional anaesthesia is the choice of anaesthesia for procedures involving the upper limb as it provides effective post-operative pain relief. Brachial plexus block (BPB) has evolved over the years as an important weapon in the armamentarium of anaesthesiologists. Local anaesthetics alone might not provide prolonged pain relief after the surgery because of its limited duration of action. Adding adjuvant to local anaesthetic is one way to prolong the analgesia. Different adjuvants have their own pros and cons. Magnesium sulphate (MgSO4), being a N-methyl-D-aspartate (NMDA) antagonist is an adjuvant to local anaesthetic in central neuraxial block, peripheral nerve blocks and fascial plane blocks. MgSO4 has been known to prolong the duration of analgesia as well as shorten the onset time of block. Different doses of perineural MgSO4 (between 100mg and 250 mg) have been used in clinical practice in brachial plexus block to increase the duration of analgesia. Studies with dose beyond 250 mg have not been used in brachial plexus block. Hence, we planned to compare the doses 125 mg, 250 mg and 500 mg of magnesium sulphate as an additive in infraclavicular brachial plexus block.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor 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 physical status I and II, Surgeries for upper limb below the elbow.

排除标准

  • Participant refusal Absolute contraindications for the block.

结局指标

主要结局

Proportion of participants with at least 150 minutes increase in the duration of analgesia when compared to the other groups.

时间窗: Every 2 hours for 24 hours

次要结局

  • To compare the onset and duration of sensory block(To compare the onset and duration of motor block)

研究者

发起方
Dr Arun Parthasarathy
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Arun Parthasarathy

Kasturba Medical College, Manipal

研究点 (1)

Loading locations...

相似试验