IRCT20161126031095N2已完成2 期
Comparison of the additive effect of dexmedetomidine and neostigmine to bupivacaine on pain intensity after cesarean section with spinal anesthesia
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 110
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
- 年龄范围
- 18 years 至 50 years（—）
- 性别
- Female
入选标准
- •Women who have had a cesarean delivery
排除标准
- •Patients who have refused to participate
- •Drug addiction
- •Have underlying diseases (moderate or severe heart, kidney, lung or nerve disease, significant scoliosis, kyphosis, obesity or blood clotting disease)
- •Patients with a height of less than 130 cm or aBody mass Index ( BMI) of more than 35
研究者
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