CTRI/2021/11/037798已完成未知
To compare the efficacy of two different doses of IV dexmedetomidine for controlling post-operative shivering in women undergoing caesarean delivery under spinal anaesthesia: a prospective, randomized, double blind, parallel group, controlled clinical trial
Koldinne Jagadeeswara Reddy0 个研究点目标入组 80 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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
- •Parturients with BMI 18-35kg/m2 undergoing
- •caesarean delivery under spinal anaesthesia
排除标准
- •Patients refusal
- •Allergy and contraindication to the study drug
- •(Dexmedetomidine)
- •Patients belonging to ASA grade III and above.
- •BMI <18 to > 35kg/m2
- •Twin / multiple pregnancy
- •History of chronic nausea or itching /pruritis
- •during pregnancy
- •Psychiatric and mentally retarded patients
研究者
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