跳至主要内容
临床试验/CTRI/2024/02/062687
CTRI/2024/02/062687尚未招募不适用

To compare ultrasound guided infraclavicular block characterstics using dexmedomitidine as adjuvant to ropivacaine and levobupivacaine for upper limb surgical intervention

Armed forces medical college, Pune1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年3月15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
80
试验地点
1
主要终点
Onset and duration of sensory and motor blockage as well as analgesia

研究概览

简要总结

The study is about comparing ultrasound guided infra clavicular block characteristicsfor upper Limb surgical intervention which will be performed in the patients who are admitted to this hospital and required a surgical intervention in the upper limb

we will be comparing dexmedetomidine with Ropivacaine(0.375%) and Levobupivacaine (0.25%) and see that which drug combination has early motor and sensory blockage and provides good analgesia.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant 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, II, III, IV
  • Age 18- 60years
  • Patients listed for surgical intervention in upper limb
  • Written informed consent of patient for the study.

排除标准

  • Age < 18 and > 60 years
  • History of allergy to local anesthetic drugs being used in the block
  • Presence of any neurological deficit in the involved limb
  • Fractures involving clavicle, shoulder region and upper 1/3 rd ofhumerus
  • Local site infection
  • Any structural deformity of the injection site
  • History of coagulopathy or patients using anticoagulants
  • Peripheral vascular disease
  • Block which failed and converted to other Anaesthesia technique.

结局指标

主要结局

Onset and duration of sensory and motor blockage as well as analgesia

时间窗: Onset and duration of sensory and motor blockage as well as analgesia | initially, every 3 minutes till the full motor and sensory block is achieved, then postop every hour until 24 hours.

次要结局

  • Intraoperative monitoring of vitals (pulse rate, blood pressure, O2saturation and(adverse effect if any), duration of analgesia, complications (if any) along with supplemented analgesia)

研究者

发起方
Armed forces medical college, Pune
申办方类型
Government medical college

研究点 (1)

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