跳至主要内容
临床试验/CTRI/2024/01/061890
CTRI/2024/01/061890尚未招募不适用

Comparison of Clinical Efficacy and Safety Profile of Hyperbaric Ropivacaine 0.75% and Hyperbaric Bupivacaine 0.5% in Spinal Anesthesia for Patients Posted for Elective Caesarean Section: An Observational Study in A Tertiary Care Hospital in Mandya.

Dr Shivakumar G1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年1月2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
Comparing the onset and duration of sensory and motor blockade.

研究概览

简要总结

The study aims in comparing the anaesthetic profile and effects of intrathecal hyperbaric ropivacaine 0.75% and hyperbaric bupivacaine 0.5% in spinal anaesthesia for elective caesarean section in a group of 80 people by using the following parameters: Primary objectives: 1. Onset and duration of sensory blockade (T6 dermatome). 2. Onset and duration of motor blockade. Secondary objectives: 1.Intraoperative hemodynamic parameters. 2.Duration of analgesia (until first dose of analgesia demand). 3.Adverse effects.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • Patients posted for elective caesarean section surgeries.
  • Age group 18 to 40 years.
  • Patients with height 150cm-180cm and weight 40kg-80kg.
  • Patients with American Society of Anaesthesiologists-Physical status (ASA-PS) grade I and II.
  • Patients willing to give informed consent to participate in the study.

排除标准

  • Patients with cardiovascular diseases or pregnancy induced hypertension and gestational diabetes mellitus.
  • Patients having increased intracranial tension, severe hypovolemia, history of bleeding diathesis and local infection.

结局指标

主要结局

Comparing the onset and duration of sensory and motor blockade.

时间窗: 24 hours

次要结局

  • To compare the anaesthetic profile and effects of intrathecal hyperbaric ropivacaine 0.75% and hyperbaric bupivacaine 0.5% in spinal anaesthesia for elective caesarean section by using the following parameters:(1.Intraoperative hemodynamic parameters.)

研究者

发起方
Dr Shivakumar G
申办方类型
Government medical college

研究点 (1)

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