跳至主要内容
临床试验/CTRI/2019/04/018390
CTRI/2019/04/018390尚未招募未知

A comparative study to assess the Efficacy of dexamethasone as an additive to 0.75% ropivacaine versus 0.75% ropivacaine alone on prolongation of duration of analgesia in ultrasound-guided single shot Supraclavicular brachial plexus block for upper limb surgeries.

Santokba Durlabhji memorial hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Patients in the age group of 18-60 years of age.
  • 2.Having ASA [American Society of Anaesthesiologists] grade I & II.
  • 3.Patient who gives informed written consent to be included in the study
  • 4.Patients scheduled for elective upper limb surgeries under supraclavicular brachial plexus block.

排除标准

  • 1.Age less than 18 years
  • 2.Having ASA [American Society of Anaesthesiologists] grade Ð?Ð?Ð? & Ð?V
  • 3.Pregnant women
  • 4.Patients in whom a written informed consent could not be taken
  • 5.Critically ill patients
  • 6.Patients with known allergy to the above drugs.
  • 7.Patients for emergency upper limb surgeries
  • 8.Patients with coagulopathies, brachial plexus neuropathies, severe bronchopulmonary disease and patients with diabetes.
  • 9.Patients with haemodynamic instability.
  • 10. Neurological deficits involving brachial plexus.
  • 11.Local infection at the injection site.

研究者

发起方
Santokba Durlabhji memorial hospital

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