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临床试验/CTRI/2024/03/063512
CTRI/2024/03/063512尚未招募Unknown

Observational study of 0.25% Levobupivacaine with Dexmedetomidine 1mcg/kg versus 0.375% Ropivacaine with Dexmedetomidine 1mcg/kg in USG guided Infra clavicular brachial plexus block administered to patients undergoing upper limb surgeries.

SREE BALAJI MEDICAL COLLEGE AND HOSPITA0 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
Unknown
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
Observational

入排标准

入选标准

  • Patients receiving 0.25% Levobupivacaine with 1mcg/kg Dexmedetomidine group L
  • Patients receiving 0.375% Ropivacaine with 1mcg/kg Dexmedetomidine group R
  • ASA Grade I and II
  • All age groups
  • Obese patients
  • Patients posted for elective surgeries

排除标准

  • ASA III and IV
  • Known case of hypersensitivity reaction to local anesthetics
  • Bleeding diathesis and Peripheral neuropathy and neuromuscular disease and psychiatric disorders
  • Local infection at the site of puncture
  • Patients with polytrauma

研究者

发起方
SREE BALAJI MEDICAL COLLEGE AND HOSPITA

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