跳至主要内容
临床试验/CTRI/2021/07/035010
CTRI/2021/07/035010尚未招募不适用

A comparative study of Dexmedetomidine and Fentanyl as adjuvants to Ropivacaine on analgesic efficacy in supraclavicular brachial plexus block

Dr Malin Debnath1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年1月8日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Onset and duration of sensory and motor block

研究概览

简要总结

This is a randomised trial, to compare analgesic efficacy of Dexmedetomidine ( 1 microgram/kg) and Fentanyl ( 1 microgram/kg) as adjuvants to Ropivacaine ( 30 ml 0.5%) in supraclavicular brachial plexus block, which will be conducted in the Department of Anaesthesiology, Regional Institute of Medical Sciences, Imphal West, Manipur, in 60 patients within the age group of 18-60 years and ASA grade I and II. Onset and duration of sensory and motor block will be recorded using Hollmen scale.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
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 AND II.

排除标准

  • Uncooperative patients/ patients refusal
  • Patients having hypertension/ diabetes mellitus/ neuropathy/ Peripheral nerve injury
  • Geriatric/ pediatric patients
  • Pregnancy and lactation
  • Patients on anticoagulants or bleeding disorders
  • Hypersensitivity to Amide group of local anesthetic agents.

结局指标

主要结局

Onset and duration of sensory and motor block

时间窗: Every 2 minutes from injecting of drugs

次要结局

未报告次要终点

研究者

发起方
Dr Malin Debnath
申办方类型
Other [self]

研究点 (1)

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