CTRI/2023/09/057280尚未招募4 期
To determine the time of onset, time to attainment of maximum level and duration of sensory and motor blockade with Levobupivacaine heavy with Dexmedetomidine versus Racemic Bupivacaine Heavy with Dexmedetomidine in Spinal Anaesthesia for Cesaean Section - NI
Rajendra Insitute of Medical Sciences, Ranchi0 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
- 4 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
- •The patient giving informed and written consent for study.
- •Primigravida posted for elective caesarean section with more than 37 weeks gestation.
- •Having singleton pregnancy.
排除标准
- •The patient not giving consent for the study.
- •Pregnancy with height less than 145cm and more than 165cm.
- •patients having any contraindications for spinal anaesthesia.
- •Pregnant women with fetal anomaly, placenta previa, abruptio placenta, placenta percreta or increta.
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