CTRI/2024/12/078329尚未招募不适用
Comparative evaluvation of spinal anaesthesia with hyperbaric solution of levobupivacaine and ropivacaine for caesarean section Randomized double-blind controlled study
Department of Anesthesia Medical college Dungarpur1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年12月30日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- onset of the sensory block
研究概览
简要总结
The aim of this study to compare the clinical efficacy of equal volume(2ml) of .75% hyperbaric ropivacaine and 0.5% hyperbaric levobupivacaine for cesarean section under spinal anaesthesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •â€¢ ASA physical status I and II, • Age between 18-35 years • At Term, Elective caesarean Section • Valid informed consent • height ranging between 150 – 170 cms • weight ranging between 50 – 90 kg.
排除标准
- •â€¢Pregnant patients having coexisting systemic disorders like neuromuscular diseases, neuronal degenerative disorder, seizure disorder, bleeding and haematological disorders, Cardiac disorders, Diabetes mellitus or gestational diabetes.
- •â€¢ Pregnant women with hepatic and renal disorders, severe Anaemia • Eclampsia, placenta previa, abruptio placenta • Parturient in active labour, Twin/ complicated pregnancy • Spinal deformities, poliomyelitis short stature.
结局指标
主要结局
onset of the sensory block
时间窗: onset of the sensory block upto 10 minutes after spinal anesthesia
次要结局
- Time to peak sensory block.(Duration of the sensory block)
研究者
Dr Mamta Damor
Govt. Medical college dungarpur
研究点 (1)
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