CTRI/2024/10/074906尚未招募不适用
Hyperbaric spinal Anaesthesia with Bupivacaine 0.25 percent for urological procedures.
GSVM1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月20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
- 60
- 试验地点
- 1
- 主要终点
- Effective sensory block ( onset and duration)
研究概览
简要总结
To use bupivacaine 0.25 % in lower urological procedures.
a) Primary aim: Effective sensory block ( onset and duration)
Effective motor block ( onset and duration)
Hemodynamic stability
b) Secondary aim:
Adverse effects if any
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
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 with American society of anaestheslogist (ASA) score: I and II 2) Elective urological endoscopic surgery.
- •Duration of surgery not exceeding 45 min.
排除标准
- •Negative consent 2) Patients with ASA score III, IV 3) Body mass index (BMI) > 30 kg/m2 4) History of obstructive sleep apnoea 5) Anticipated difficult intubation 6) Spine deformities, previous spine surgery 7) Coagulation abnormalities 8) Allergy to local anaesthetics.
结局指标
主要结局
Effective sensory block ( onset and duration)
时间窗: Base line, 4 weeks, 8 weeks.
Effective motor block ( onset and duration)
时间窗: Base line, 4 weeks, 8 weeks.
Hemodynamic stability
时间窗: Base line, 4 weeks, 8 weeks.
次要结局
- Adverse effects(Base line, 4 weeks, 8 weeks.)
研究者
NEHA KUMAR
GSVM MEDICAL COLLEGE, KANPUR
研究点 (1)
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