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临床试验/CTRI/2025/01/078986
CTRI/2025/01/078986尚未招募不适用

A COMPARATIVE EFFICACY BETWEEN 0.5 percent ROPIVACAINE HEAVY VS 0.5 percent BUPIVACAINE HEAVY FOR INTRATHECAL ANAESTHESIA IN CEASAREAN SECTION - A PROSPECTIVE, DOUBLE-BLIND RANDOMISED CONTROLLED TRIAL

Heritage Institute Of Medical Sciences1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2025年1月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
132
试验地点
1
主要终点
To compare the duration of analgesia between Ropivacaine and Bupivacaine in intrathecal anaesthesia

研究概览

简要总结

This study is designed to compare the duration of analgesia between Ropivacaine and Bupivacaine intrathecal anaesthesia and also to compare the onset and duration of sensory and motor block, hemodynamic changes and the side effects in both groups

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
21.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • Pregnancy (over 37 weeks and less than 42weeks).

排除标准

  • Patients refusal Infection at the site of injection Coagulopathy or any other bleeding diathesis Increased intracranial pressure Known case of any hypersensitive reactions to local anaesthetics.

结局指标

主要结局

To compare the duration of analgesia between Ropivacaine and Bupivacaine in intrathecal anaesthesia

时间窗: Every 15 minutes during intra operative

次要结局

  • To compare the onset & duration of sensory & motor block , hemodynamic changes & side effects in both the groups(Every 15 minutes till 3 hours & then every 30 mins till 12 hours)

研究者

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

Dr Shilpi Pandey

Heritage Institute Of Medical Sciences , Varanasi

研究点 (1)

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