跳至主要内容
临床试验/CTRI/2021/05/033452
CTRI/2021/05/033452尚未招募不适用

A COMPARATIVE CLINICAL STUDY BETWEEN NALBUPHINE AND FENTANYL AS ANAJUVANT TO ROPIVACAINE IN ULTRASOUND GUIDED SUPRACLAVICULAR BRACHIAL PLEXUSBLOCK

Dr Anitha A1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年10月5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
Time to onset of sensory and motor block.

研究概览

简要总结

To compare the effect of Nalbuphine and Fentanyl as an adjuvant to Ropivacaine in

ultrasound guided interscalene brachial plexus block with respect to

  1. To assess the onset and duration of sensory and motor blockade.

  2. To assess duration of analgesia.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • American Society of Anesthesiologist physical status 1 and 2.

排除标准

  • Any neurological deficit, peripheral neuropathies, myopathies or chronic pain in the operative limb.
  • History of anaphylaxis to local anaesthetics or known allergy to any of the study drugs to be used.
  • Any history of bleeding diathesis or coagulation abnormalities.
  • Any skin infection or local disease at the needle insertion site.
  • BMI more than 35kg/sq-m, failure to achieve adequate block within 30 mins of administration.

结局指标

主要结局

Time to onset of sensory and motor block.

时间窗: Time to onset of sensory and motor block. | Duration of sensory and motor block. | Duration of analgesia

Duration of sensory and motor block.

时间窗: Time to onset of sensory and motor block. | Duration of sensory and motor block. | Duration of analgesia

Duration of analgesia

时间窗: Time to onset of sensory and motor block. | Duration of sensory and motor block. | Duration of analgesia

次要结局

  • Pain scores(Adverse effects- Hypotension, Bradycardia,)

研究者

发起方
Dr Anitha A
申办方类型
Other [self]

研究点 (1)

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