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临床试验/CTRI/2024/08/072515
CTRI/2024/08/072515尚未招募4 期

Comparison of Dexmedetomidine and Dexamethasone used as an Adjuvant to Ropivacaine in Ultrasound-Guided Supraclavicular Brachial Plexus Block.

Dr Umesh N P1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年8月20日最近更新:

试验速览

阶段
4 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 the onset and duration of motor and sensory block between dexmedetomidine and dexamethasone as an adjuvant to ropivacaine in ultrasound-guided supraclavicular brachial plexus block.

研究概览

简要总结

Study is initiated to compare the onset and duration of motor and sensory block between dexmedetomidine and dexamethasone as an adjuvant to ropivacaine in ultrasound guided supraclavicular brachial plexus block will be assesed and recorded and to compare the sedation, duration of analgesia, side effects during the study

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients of both sexes aged ≥18 yrs.
  • 2.Patients undergoing elective upper limb surgeries.
  • 3.ASA-PS I and II patients.
  • 4.Patients who are willing to participate in the study with informed consent.

排除标准

  • 1.Infection at site of injection.
  • 2.Patients who have peripheral neuropathy.
  • 3.Presence of 1st,2nd and 3rd degree heart block.
  • 4.Patients who are pregnant.
  • 5.Patients who have coagulopathies.
  • 6.Patients who have allergy or hypersensitivity to local anaesthetic drugs.

结局指标

主要结局

To compare the onset and duration of motor and sensory block between dexmedetomidine and dexamethasone as an adjuvant to ropivacaine in ultrasound-guided supraclavicular brachial plexus block.

时间窗: 24 HOURS

次要结局

  • 1.To compare the sedation during intraoperative period.(2.To compare the duration of analgesia in post operative period.)

研究者

发起方
Dr Umesh N P
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Umesh N P

Mandya institute of medical sciences

研究点 (1)

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