CTRI/2021/07/034963尚未招募未知
Comparison of efficacy and safety of nalbuphine, dexmedetomidine and tramadol for treatment of post-spinal shivering in pregnant women undergoing Caesarean section
Government Institute of Medical sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
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
入选标准
- •1. Patients from obstetrics group aged between 20â??40 years of ASA grade I and II undergoing caesarean section.2. Patients who will give a valid informed written consent.
- •3.Patients who will develop shivering of grade 3or4.
排除标准
- •1. Patients of age group between 20-40belonging to ASA grade III and IV.
- •2. Patients with known hypersensitivity to tramadol, dexmedetomidine and nalbuphine.
- •3. Patients who will not give valid informed consent.
- •4. Patients who will have shivering before spinal anaesthesia.
- •5. Patients who will have shivering before delivery.
- •6. Contraindication of spinal anaesthesia.
研究者
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