CTRI/2022/08/044691尚未招募4 期
Randomised double blinded prospective study to compare the effects of 0.75% Ropivacaine heavy and 0.5% Bupivacaine heavy in subarachnoid block for caesarean delivery in obstetric patients
Mytily0 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
- •Obstetric patients coming for elective caesarean section
- •Age group of 20-40 years
- •ASA 1 & ASA 2 patients
- •Full term pregnant patients
- •Patients with Single live intrauterine fetus
排除标准
- •1.Patients who refuse
- •2.Emergency surgeries
- •3.Age group <20 or >40 years of age
- •4.ASA 3 & ASA 4 patients
- •5.Pre term patients
- •6.Multiple pregnancy (twin or more gestation)
- •7.Associated comorbid conditions( PIH, GDM, Anaemia, Heart disease)
- •8.Bleeding diathesis patients
- •9.Fetal indication for caesarean delivery
研究者
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