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
研究点 (1)
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