CTRI/2026/04/107397尚未招募不适用
A randomized controlled trial of comparing the effects of different adjuvants to hyperbaric Bupivacaine in subarachnoid block in patients undergoing lower limb orthopedic surgeries
Air Force Hospital1 个研究点 分布在 1 个国家目标入组 138 人开始时间: 2026年4月6日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 138
- 试验地点
- 1
研究概览
简要总结
Based on current evidence, dexmedetomidine 5 µg as an intrathecal adjuvant to 0.5 hyperbaric bupivacaine offers several advantages
Faster onset of both sensory and motor blockade
Prolonged block duration and postoperative analgesia
Better hemodynamic stability
Minimal side effects compared to opioids like fentanyl or nalbuphine
It is a superior and safe adjuvant that enhances the quality and duration of spinal anesthesia in lower abdominal and lower limb surgeries
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Double
入排标准
- 年龄范围
- 18.00 Year(s) 至 99.00 Year(s)（—）
- 性别
- All
入选标准
- •Age more than 18 yrs.
排除标准
- •Infection at the site of injection Coagulopathy or anticoagulation Congenital anomalies of the lower spine Any preexisting neuropathy History of allergy to local anaesthetics.
研究者
Dr Shaik Nagoor Vali
7 AIR FORCE HOSPITAL
研究点 (1)
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