CTRI/2021/06/034193尚未招募不适用
A Study To Test The Efficacy And Safety Of Pre Procedure Ultrasound Guided Paramedian Technique As Compared To Conventional Landmark Guided Paramedian Technique In Administering Spinal Anesthesia
Shri BM Patil Medical College1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2021年6月30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
- 1.To compare number of needle passes in both groups (i.e. withdrawal and redirection of spinal needle without exiting the skin)
研究概览
简要总结
To study the efficacy and safety of pre-procedure ultrasound guided paramedian technique as compared to conventional landmark guided paramedian technique in administering spinal anesthesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Adaptive randomization, such as minimization
- 盲法
- Open Label
入排标准
- 年龄范围
- 50.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •All consenting patients planned for elective lower abdomen, pelvic and lower limb surgeries under spinal anaesthesia
- •Age 50 years and above
- •ASA grade I and II.
排除标准
- •Patients with known allergy to local anaesthetic drug
- •Patients with coagulopathies
- •Signs of infection at site of injection
- •Patient refusal
- •Neurological disorder or deficit.
结局指标
主要结局
1.To compare number of needle passes in both groups (i.e. withdrawal and redirection of spinal needle without exiting the skin)
时间窗: At 10, 20 and 30 minutes after Spinal Anaesthesia
2.To compare number of needle attempts in both groups (i.e. number of times the spinal needle was withdrawn from skin and reinserted)
时间窗: At 10, 20 and 30 minutes after Spinal Anaesthesia
次要结局
- To compare incidence of blood in spinal needle in both groups(Immediately after the procedure)
研究者
研究点 (1)
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