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临床试验/CTRI/2026/03/106474
CTRI/2026/03/106474尚未招募不适用

Comparison of Magnesium sulphate and Dexamethasone as adjuvants to Ropivacaine in ultrasound guided brachial plexus block for postoperative analgesia in patients undergoing upperlimb surgeries A randomised controlled trial

MOSC MEDICAL COLLEGE1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年3月28日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
试验地点
1
主要终点
To compare the duration of postoperative analgesia of ropivacaine and magnesium sulphate with ropivacaine and dexamethasone in brachial plexus blocks using numerical rating scale(NRS) for patients undergoing elective upper limb surgeries under general anaesthesia.

研究概览

简要总结

To compare the duration of postoperative analgesia with 0.75% ropivacaine (20ml) and magnesium sulphate 250mg (1ml) versus 0.75%ropivacaine (20ml)and dexamethasone 4mg (1ml) in ultrasound guided brachial plexus blocks in patients undergoing elective upper limb surgeries under general anaesthesia and to compare the pain score and total requirement of analgesics over 24 hours postoperatively. Duration of analgesia will be calculated from the time of administration of the block to the time of rescue analgesia. Pain score will be calculated with the help of numerical rating scale (NRS) and when the patient has a pain score >/=3, analgesic will be started with paracetamol at a dose of 15mg/kg 8th hourly. Pain score will be assessed every 4th hourly. If the pain does not subside, tramadol 100mg will be added and at the end of 24 hours total analgesic requirement is calculated

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 70.00 Year(s)(—)
性别
All

入选标准

  • Age: 18 -70 years
  • ASA physical status I and II patients
  • Body mass index (BMI) of 18-30 kg/m2
  • Patients undergoing elective upper limb surgeries under general anaesthesia with brachial plexus block.

排除标准

  • Patient Refusal
  • Allergy to local anesthetic
  • Altered coagulation profile
  • Infection at site of injection
  • Failure of block.

结局指标

主要结局

To compare the duration of postoperative analgesia of ropivacaine and magnesium sulphate with ropivacaine and dexamethasone in brachial plexus blocks using numerical rating scale(NRS) for patients undergoing elective upper limb surgeries under general anaesthesia.

时间窗: Patient will be assessed for postoperative analgesia using numerical rating scale every 4th hourly for 24 hours

次要结局

  • To compare the total requirement of analgesics over 24 hour period postoperatively in patients undergoing upper limb surgeries under general anaesthesia with brachial plexus block using magnesium sulphate & dexamethasone as adjuvants to ropivacaine(Every 4th hourly for 24 hours)
  • To compare the pain score at 4 hour intervals postoperatively in patients undergoing elective upper limb surgeries under general anaesthesia with brachial plexus block using magnesium sulphate & dexamethasone as adjuvants to ropivacaine(Every 4th hourly for 24 hours)
  • To compare the various hemodynamic parameters in patients undergoing elective upper limb surgeries under general anaesthesia with brachial plexus block using magnesium sulphate & dexamethasone as adjuvants to ropivacaine(Every 4th hourly for 24 hours)

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Jishina Issac

MOSC medical college kolenchery

研究点 (1)

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