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临床试验/CTRI/2025/10/095958
CTRI/2025/10/095958尚未招募不适用

Comparison of two doses of Dexmedetomidine as an adjuvant to Bupivacaine 0.5% in USG guided Supraclavicular Brachial Plexus Block: A Double Blind Randomised controlled study

School of medical sciences and research Sharda hospital Sharda university1 个研究点 分布在 1 个国家目标入组 99 人开始时间: 2030年8月14日

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
99
试验地点
1
主要终点
To compare the efficacy of two doses of Dexmedetomidine as an adjuvant to Bupivacaine 0.5% in ultrasound-guided supraclavicular brachial plexus block in upper limb surgery

研究概览

简要总结

This randomised double blinded controlled study aims to compare the two doses of Dexmedetomidine as an adjuvant to Bupivacaine 0.5% in USG guided supraclavicular brachial plexus block.A total of 60 Patients will be enrolled and divided in to three groups.

The primary outcome will be assessed by hemodynamic parameters like HR,SBP,DBP,MAP,SPO2 at baseeline and at every 5mins for 1hour and 15mins till completion of surgery.The secondary outcome will be assessed using Pinprick method,modified bromage scsle,Sedation score,VAS score,complications like local anaaesthesia toxicity,phrenic nerve palsy,subcutaneous emphysema and pneumothorax.The goal is to evaluate comparison of efficacy of analgesia in two doses of Dexmedetomidine to Bupivacaine in upper limb surgeries

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 65.00 Year(s)(—)
性别
All

入选标准

  • Patients undergoing elective upper limb surgery.
  • Age between 18 to 65 years.
  • ASA physical status class 1 and 2.

排除标准

  • History of allergy or hypersensitivity to local anaesthetic Local infection at the site of injection Refusal to consent Patients with coagulation disorders Pregnancy Morbid obesity History of coronary artery disease, chronic renal and hepatic disease Seizure disorder Psychiatric disease.

结局指标

主要结局

To compare the efficacy of two doses of Dexmedetomidine as an adjuvant to Bupivacaine 0.5% in ultrasound-guided supraclavicular brachial plexus block in upper limb surgery

时间窗: To compare the duration of analgesia

次要结局

  • 1. To compare the onset and duration of sensory and motor block 2. To compare the rescue analgesic requirements in 24hrs(3.To compare the intraoperative sedation score)

研究者

发起方
School of medical sciences and research Sharda hospital Sharda university
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Adithya V

School of medical sciences and research Sharda hospital Sharda university

研究点 (1)

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