CTRI/2022/08/044710尚未招募3 期
A Randomised control trial comparing the efficacy of intravenous oxytocin and intravenous carbestocin in haemodynamic stability of patients undergoing caesarean section under spinal anesthesia
Sabari C G S0 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
- 3 期
- 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)Age between 18 to 40 years.
- •2)American Society of Anaesthesiologists physical status II
- •3)Patients undergoing elective caesarean section under regional anaesthesia.
- •4)Provides Consent.
排除标准
- •1)Presence of hypertension, preeclampsia, cardiac, renal or liver diseases, epilepsy and patients undergoing general anaesthesia.
- •2)Patient who are unable or unwilling to give consent.
- •Ã¢â?¬Â¢Women with history of hypersensitivity to carbetocin.
- •Ã¢â?¬Â¢Patients who do not fulfil inclusion criteria.
研究者
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