CTRI/2023/01/048768尚未招募4 期
A Randomized prospective study comparing efficacy of 0.5% Hyperbaric Levobupivacaine with 0.5% Hyperbaric Bupivacaine for subarachnoid block in Orthopedic lower limb surgeries
TATA MAIN 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
- 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
- •Adult (Age >= 18 - 60 Years) undergoing orthopedic lower limb surgeries under Subarachnoid block
- •2 . ASA grade I and II
- •3.Anticipated Duration of surgery 120 minutes
排除标准
- •1. Patient refusal to participate in study
- •2. Contraindication to subarachnoid block
- •3. Patients with height < 150 cm or > 180 cm
- •4. Patients with BMI >= 30
- •5. Patient with history of allergy to local anaesthetics
研究者
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