Compare analgesic efficacy of USG guided pericapsular nerve group block versus suprainguinal fascia iliaca block for post operative pain relief in hip surgery
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Duration of pain relief assessment
研究概览
简要总结
Written informed consent will be taken from patients undergoing hip surgery under SAB between 25-75 years
Patients will be randomly allocated into two groups
Group A will receive pericapsular nerve group block and Group B will receive suprainguinal fascia iliaca block
To avoid bias patient and observer will be unaware of the type of block given
Time to first requirement of analgesics will be noted
Total analgesic requirement in 24 hours, VAS score assessment for severity of pain, patient’s satisfaction score and procedure or drug related complications noted
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Double
入排标准
- 年龄范围
- 25.00 Year(s) 至 75.00 Year(s)(—)
- 性别
- All
入选标准
- •ASA 1-3,Patients scheduled for unilateral hip surgery.
排除标准
- •Patient refusal
- •Surgery more than 150 min
- •Coagulation or bleeding disorder
- •Allergy to local anaesthetics
- •Presence of other fracture requiring surgery
- •Morbid obesity
- •Pre-existing uncontrolled cardiovascular disease, renal failure, hepatic failure.
结局指标
主要结局
Duration of pain relief assessment
时间窗: Time to first requirement of analgesics will be noted post operative till 24hours
次要结局
- 1. Total analgesic requirement in 24 hrs postoperatively.(2.Intensity of pain relief assessment by VAS score at 0,2,4,8,12,24 hours.)
研究者
Simran Rana
Pt jnm medical college raipur cg
