CTRI/2020/06/025823尚未招募未知
â??A comparative study of safety and efficacy of 0.5%Ropivacaine combined with either Dexmedetomidine orClonidine as adjuvant ; given as USG guidedsupraclavicular brachial plexus block, in patientsundergoing elective upper limb orthopaedic surgery.â??
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
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
- •ASA I & II of body weight 30 to 80 kg, undergoing upperlimb orthopaedic surgery of less than two hours duration.
- •Free from any associated chronic systemic illness.
排除标准
- •Uncooperative patient
- •Pregnant or lactating mother
- •Neurological deficit in operative limb with chronic pain or on long term analgesics
- •Patient having hypersensitivity or contraindication to Ropivacaine/ Dexmedetomidine/ Clonidine
- •Local pathology at the site of injection
- •All disability limiting the performance of block
研究者
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