PACTR201306000510382尚未招募未知
Transient Neurologic symptoms following spinal lignocaine and bupivacaine for caesarean delivery in mulago hospital, a randomised trial.
Dr Aggrey Lubikire(self)0 个研究点目标入组 180 人开始时间: 2013年2月26日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 180
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 Year(s) 至 40 Year(s)（—）
- 性别
- Female
入选标准
- •only ASA 1 and 2 and E , patients above 18 and provide informed consent to participate in the study will be enrolled.
排除标准
- •Patients with previous neurologic deficits, periperal neuropathy like diabetes, previous back injuries.
- •Failed spinal :patients who receive spinal blockade with either Lignocaine or Bupivacaine, and the drug fails to take, then get general anaesthesia will be excluded.
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