CTRI/2021/11/038119招募中4 期
To compare the sedative effect of subarachnoid block with and without intravenous midazolam using BIS monitoring in patients undergoing lower limb surgeries-A randomized controlled trial
AIIMS New Delhi0 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
- 招募中
- 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
- •Patients of age 20-60 years, either sex, American Society of Anesthesiologists (ASA) physical status I and II undergoing surgery (min duration of 90min) under SAB or combined spinal epidural anesthesia (CSEA) will be enrolled for the study.
排除标准
- •Patients with any known allergy to study drugs, contraindication for central neuraxial block, obesity (body mass index, [BMI] >35 kg/m2), neurological or psychiatric disease on concurrent medication and refusal will be excluded from the study.
研究者
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