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临床试验/CTRI/2025/03/082208
CTRI/2025/03/082208尚未招募2/3 期

Comparison of Dexamethasone 4 mg and 8 mg as an Adjuvant to 0.5% Bupivacaine in Supraclavicular Brachial Plexus Block for Upper Limb Surgeries

Government of Gujurat1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年3月18日最近更新:

试验速览

阶段
2/3 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 duration and onset of sensory and motor blockage in both group

研究概览

简要总结

Brachial plexus block has evolved as an important tool as a safe alternative to general anaesthesia for upper limb surgery and peri-operative analgesia.Bupivacaine is a potent local anaesthetic drug  widely used for prolonged local and regional anaesthesia.Many additives can be added to local anaesthetics such as opioids, clonidine, tramadol, dexmedetomidine, dexamethasone that have been used to increase the duration of the block, to improve the postoperative pain management.In this study we compare duration of analgesia, onset and duration of sensory and motor block and hemodynamic parameters in supraclavicular brachial plexus block with Dexamethasone 4mg and 8mg as an adjuvant to 0.5% Bupivacaine.

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 60.00 Year(s)(—)
性别
All

入选标准

  • ASA grade : I,II,III
  • Elective upper limb surgeries under supraclavicular brachial plexus block.
  • Patient giving consent.

排除标准

  • Any bleeding disorder and patient on anticoagulants
  • Contralateral lung injury and rib fracture
  • Pre-existing neuropathy involving the surgical limb
  • Local infection at the injection site
  • History of allergy to local anaesthetic and dexamethasone
  • Patients with a history of peptic ulcer disease, hepatic or renal failure (contraindication to steroids)
  • Pregnant women
  • Systemic use of corticosteroids for 2 weeks or longer within 6 months of surgery
  • Unwilling patient.

结局指标

主要结局

To compare duration and onset of sensory and motor blockage in both group

时间窗: To compare duration and onset of sensory and motor blockage in both group starting from baseline to every 3 min with 3 point scale method.

次要结局

  • To compare hemodynamic parameter intraoperative and To compare complication intraoperative and postoperative in both group(24 hour postoperative)

研究者

发起方
Government of Gujurat
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Jigneshkumar chauhan

B.J. Medical College and Civil Hospital , Ahmedabad

研究点 (1)

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