CTRI/2024/01/061853尚未招募4 期
A prospective randomised controlled study compairing equipotent dose of hyperbaric Ropivacaine and hyperbaric levo Bupivacaine in lower limb orthopaedic surgery under subarachnoid block. - NI
RIMS, RANCHI0 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
- 4 期
- 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
- Interventional
入排标准
入选标准
- •1) 18 to 65 years of either sex
- •2) Weight of 45 to 75 kgs
- •3)Height of 150 to 180cms
- •4) Patients undergoing lower limb orthopaedic surgery
- •5) ASA grade I & II
排除标准
- •1)Patient unwilling
- •2)Any bleeding disorder and patient on anticoagulants.
- •3) Neurological and musculoskeletal disease.
- •4) History of any allergy to local anaesthetic agents and signs of allergy to lidocaine test dose.
- •5)Significant history of drug/alcohol abuse
- •6) Patients with contradindication for regional anaesthesia
研究者
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