A randomized controlled trial comparing intrathecal hyperbaric Levobupivacaine 0.5 and hyperbaric Ropivacaine 0.75 for elective caesarean section : Analysis of block characteristics when an equipotent dose is used
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 66
- 试验地点
- 1
- 主要终点
- Onset, duration of sensory block
研究概览
简要总结
We will be conducting a double blind randomized controlled study in which we will compare the motor and sensory blocks of two local anesthetic agents.
We will include a total of 66 pregnant patients who will be scheduled for elective caesarean section under spinal anesthesia.
We will observe the onset and duration of sensory as well as motor block characteristics along with hemodynamic effects and complications of both study drugs.
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
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant females,
- •40 years age group, ASA 1 & 2, scheduled for elective caesarean section under spinal anesthesia.
排除标准
- •History of allergy to local anesthetics Uncontrolled systemic comorbid illness Any obstetric complications BMI > 30.
结局指标
主要结局
Onset, duration of sensory block
时间窗: Baseline | Immediately after spinal anesthesia | Every 2 minutes for 10 minutes | Every 5 minutes for next 10 minutes | Every 30 minutes till regression of sensory level to L5
Onset, duration of motor block
时间窗: Baseline | Immediately after spinal anesthesia | Every 2 minutes for 10 minutes | Every 5 minutes for next 10 minutes | Every 30 minutes till regression of sensory level to L5
Haemodynamic effects
时间窗: Baseline | Immediately after spinal anesthesia | Every 2 minutes for 10 minutes | Every 5 minutes for next 10 minutes | Every 30 minutes till regression of sensory level to L5
次要结局
- Foetal effects(Postoperative analgesia)
研究者
ABHISHEK CHATTERJEE
Tata Main Hospital