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临床试验/CTRI/2025/01/079126
CTRI/2025/01/079126尚未招募1/2 期

Study of Dexamethasone as an Adjuvant to Levobupivacaine for Analgesic efficacy in Infraclavicular Brachial Plexus Block in patients undergoing Upper Limb Surgery

Dr Sarvjeet Kaur1 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5日最近更新:

试验速览

阶段
1/2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Duration of sensory and motor Block

研究概览

简要总结

We aim to evaluate the role of perineural dexamethasone as an adjuvant along with levobupivacaine in infraclavicular brachial plexus block for upper limb surgeries. The study will be conducted in a randomized, controlled manner in the Department of Anaesthesiology, GGS Medical College and Hospital, Faridkot on patients of age between 18 to 60 years, American Society of Anaesthesiologists Grade I and II, scheduled to undergo below elbow surgeries. The total patients 60 will be randomly allocated into groups of 30 patients each.

Group LB:-will receive 25 ml drug (24 ml 0.5% levobupivacaine + 1 ml NS)

Group LD:- will receive 25 ml drug (24ml 0.5% levobupivacaine plus 1 ml dexamethasone(4mg)

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

  • Patients with American Society of Anaesthesiologists grade I and II
  • Patients between age of 18-60 years, giving valid informed and written consent.

排除标准

  • Patients with inability to comprehense pain
  • Patients who have allergy to study drugs
  • Patients with local site infections
  • Patients having coagulation abnormalities
  • Patients who are on prolonged analgesics.

结局指标

主要结局

Duration of sensory and motor Block

时间窗: Every 1 hr till it resolves

次要结局

  • Quality of analgesia(Every 1 hr till it resolves)

研究者

发起方
Dr Sarvjeet Kaur
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Sarvjeet Kaur

GGSMCH, Faridkot

研究点 (1)

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