跳至主要内容
临床试验/CTRI/2026/04/109244
CTRI/2026/04/109244尚未招募不适用

Efficacy and safety of hyperbaric levobupivacaine vs. hyperbaric bupivacaine in spinal anaesthesia for caesarean section

K S Hegde Medical Academy1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年5月3日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
80
试验地点
1

研究概览

简要总结

This randomized controlled observational study compares the efficacy and safety of hyperbaric levobupivacaine with fentanyl versus hyperbaric bupivacaine with fentanyl for spinal anaesthesia in elective caesarean sections.The primary objective is to evaluate the onset and duration of sensory and motor block and comparison of maternal hemodynamic parameters. Pregnant women over 18 years undergoing elective caesarean delivery will be randomly allocated to either group.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • 1.Pregnant ladies aged above 18 years undergoing lower segment caeserean section under spinal anaesthesia using 25G Quincke Babcock needle 2.ASA physical status II 3.Singleton pregnancy 4.Height of 150 cm or more.

排除标准

  • 1.History of allergy to study drugs 2.Pregnant females with neurological deficits of lower extremities 3.Complicated pregnancy 4.Conversion of spinal to general anaesthesia intraoperatively 5.Duration more than 2hours.

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Maansi Kolle

K S HEGDE MEDICAL ACADEMY

研究点 (1)

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