EVALUATION OF EFFECTIVENESS OF PERICAPSULAR NERVE GROUP(PENG) BLOCK WITH ROPIVACAINE VS ROPIVACAINE WITH DEXMEDETOMIDINE IN PATIENTS WITH HIP FRACTURES - A RANDOMIZED CONTROLLED STUDY
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- To compare the onset of pain relief & reduction in pain score(VAS)during the positioning of patients for central neuraxial blockade with 0.25% ropivacaine 20ml and 0.25% ropivacaine 20ml and dexmedetomidine 25 mcg
研究概览
简要总结
The study is a double blinded randomised control study to compare the analgesic effectiveness of Pericapsular nerve group (PENG) block with ropivacaine vs ropivacaine with dexmedetomidine in patients with hip fractures.The study will be conducted on patients above 18 years of age and belonging to ASA 1,2,3 with hip fractures
The study will be conducted for a period of 18 months in patients with hip fractures coming to Sri Venkateshwaraa medical college ,hospital and research centre .The primary objective is to compare the onset of pain relief and reduction in pain score(VAS) during the positioning of patients for central neuraxial blockade between the two groups.
The secondary objective is to access the duration of post operative pain relief in both groups and to access the total analgesic requirements for 24 hours.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 90.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients belonging to ASA grade 1,2 and 3 with hip fractures, posted for surgery under spinal anaesthesia who are unable to sit due to pain in the hip joint.
- •Patients of either sex above 18 years of age.
排除标准
- •Patients with hemorrhagic diasthesis, neurocognitive disorders,spinal deformities, psychiatric disorders.
- •Patients with allergy to study drug.
- •Patients with polytrauma, infection over injected site.
结局指标
主要结局
To compare the onset of pain relief & reduction in pain score(VAS)during the positioning of patients for central neuraxial blockade with 0.25% ropivacaine 20ml and 0.25% ropivacaine 20ml and dexmedetomidine 25 mcg
时间窗: duration of onset of pain relief will be noted at 5,10,15,20,30 minutes after the block
次要结局
- To assess the duration of post operative pain relief in both groups & to assess the total analgesic requirements for 24 hours(18 months)