临床试验/CTRI/2022/10/046717

CTRI/2022/10/046717已完成不适用

Comparison of 0.75% hyperbaric ropivacaine versus 0.5% hyperbaric bupivacaine in spinal anaesthesia for elective surgery

Bhabha Atomic Research Centre1 个研究点分布在 1 个国家目标入组 50 人开始时间: 2022年10月27日最近更新: 2024年2月16日

试验速览

阶段: 不适用
状态: 已完成
发起方: Bhabha Atomic Research Centre
入组人数: 50
试验地点: 1
主要终点: To study duration of action of hyperbaric ropivacaine and hyperbaric bupivacaine.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

50 Patients posted for elective infra-umbilical procedures will be grouped into 2 groups, Ropivacaine(25) versus Bupivacaine(25). Spinal anaesthesia will be performed and the following parameters will be studied.

Time taken to achieve maximum Sensory block.

Time taken to achieve Complete Motor block.

Intra-operative Hemodynamics.

Time taken for 5 segment regression of sensory block.

Time taken for regression of Motor block to Modified Bromage 1.

Side effects.

研究设计

研究类型: Interventional
分配方式: Other
盲法: Participant and Investigator Blinded

入排标准

年龄范围: 18.00 Year(s) 至 60.00 Year(s)（—）
性别: All

入选标准

•Patients aged 18-60 years, ASA grade I-II undergoing elective infra-umbilical surgeries, less than 2hours, under spinal anaesthesia.

排除标准

•Patient refusal Pregnancy Allergy to local anesthetic drugs Any other contra indications to spinal anaesthesia.

结局指标

主要结局

To study duration of action of hyperbaric ropivacaine and hyperbaric bupivacaine.

时间窗: 24hours

次要结局

To study(1.Time taken to achieve maximum sensory blockade.)

研究者

发起方

Bhabha Atomic Research Centre

申办方类型

Other [DNB Training Central Government Hospital]

研究点 (1)

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