跳至主要内容
临床试验/CTRI/2020/09/027929
CTRI/2020/09/027929尚未招募不适用

Comparative evaluation of analgesic efficacy of different dose of Dexamethasone as adjuvant to Levobupivacaine in ultrasound guided brachial plexus block in upper limb surgeries.

Department of Anaesthesiology1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2020年9月22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
126
试验地点
1
主要终点
Duration of effective post operative analgesia

研究概览

简要总结

This study will compare the analgesic efficacy of two dose of Dexamethasone as adjuvant to Levobupivacaine in ultrasound guided supraclavicular brachial plexus block for upper limb surgeries

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

  • Patients belonging to ASA I and II Mallampati grade 1 and 2 posted for upper limb surgeries.

排除标准

  • Coagulopathies (INR>1.5) Infection at site of block A compromised lung function at opposite side of block like pneumothorax hemothorax pneumonectomy Hypersensitivity to Local anaesthetics or Dexamethasone Patients refusal or inability to communicate.

结局指标

主要结局

Duration of effective post operative analgesia

时间窗: 24 hours post operative period

次要结局

  • Time of onset of sensory and motor block
  • Duration of sensory and motor block(24 hours post operative period)
  • VAS score(24 hours post operative period)
  • Incidence of post operative nausea vomiting(24 hours post operative period)
  • Rate of infection neurologic complication hyperglycemia(24 hours post operative period)

研究者

发起方
Department of Anaesthesiology
申办方类型
Government medical college

研究点 (1)

Loading locations...

相似试验