CTRI/2024/12/077717招募中不适用
A prospective randomized-controlled trial study to study the duration of Post operative analgesia of a combination of Low Dose Spinal Anaesthesia and Lumbar and Sacral Plexus Blocks in Lower Limb Surgery
Vikhe Patil Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年12月23日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Duration of post operative analgesia
研究概览
简要总结
To compare the duration of post operative analgesia of a combination of lumbar and sacral plexus blocks and low dose sub-arachnoid block in lower limb surgery as compared to combined sub-arachnoid and epidural blocks in standard doses.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 99.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients undergoing lower limb surgeries including trauma surgery
- •Age above 18.
排除标准
- 未提供
结局指标
主要结局
Duration of post operative analgesia
时间窗: Duration of post operative analgesia
次要结局
- Analgesic requirement(48 hours)
研究者
Dr Nikhil Karkhanis
Vikhe Patil Institute of Medical Sciences
研究点 (1)
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