IRCT20120915010841N20已完成2 期
Comparison of 10 and 12 mg doses of intrathecal bupivacaine %0.5 on sensory block level and postdural puncture headache in patients under repeated spinal after failed spinal anesthesia in C/S.
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 40
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 48 years（—）
- 性别
- Female
入选标准
- •Patient's consent to participate in the study
- •No history for diabetes, high blood pressure, heart disease
- •Patients who have failed spinal anesthesia and undergo general anesthesia
排除标准
- •Patients with contraindications of spinal anesthesia (ICP increase, shock, history of coagulation problems ..)
研究者
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