CTRI/2019/07/020231尚未招募2 期
To estimate the effective dose of phenylephrine infusion for preventing spinal anaesthesia induced hypotension in elective caesarean deliveries, a randomized control trial.
DEVDUTTA RAIGUR0 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
- 2 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
- •>37 weeks gestation, ASA grade 2 females posted for elective caesarean delivery.
排除标准
- •1. American Society of Anaesthesiologists (ASA) grade III and IV pregnant females.
- •2. Unwilling patients.
- •3. Patients with any uncontrolled systemic disorder like diabetes, hypertension, pre-eclampsia, HELLP syndrome, hepatic or renal impairment, severe airway disorder, seizure disorder or eclampsia, any cardiac diseases.
- •4. Patients with known hypersensitivity or allergy to either Phenylephrine.
- •5. Patients with any contraindication for undergoing spinal anaesthesia.
研究者
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