COMPARISON BETWEEN PERICAPSULAR NERVE GROUPBLOCK AND FASCIA ILIACA BLOCK FOR POSITIONING IN HIPFRACTURE PATIENTS BEFORE NEURAXIAL BLOCK– ARANDOMIZED CONTROLLED PILOT STUDY
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- To assess and compare the analgesic efficacy of USG guided pericapsular nerve group (PENG) block with fascia iliaca compartment block (FICB) using VAS score during positioning of hip fracture patients within 30 minutes before neuraxial block.
研究概览
简要总结
The study is a randomized controlled trial-a pilot study to compare analgesic efiicay between pericapsular nerve group block and fascia iliaca block for positioning in hip fracture patients before neuraxial block using VAS score,sitting angle, anaesthetist satisfaction, patient satisfaction, 24 hour toatal analgesic cosumption. The drug used is 20ml 0.25% ropivacaine in each group,and procedure will be ultrasound guided.There is no comparitive study between these two block ,hence investigator proposed this trial
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 80.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients with age above 18 years, undergoing surgery for hip fracture under neuraxial block.
排除标准
- •Patient refusal.
- •Any contraindication to neuraxial block like coagulopathy, local infection, increased ICP, spine trauma etc.
- •Known allergy to local anaesthetic drugs.
- •Peripheral neuropathy.
- •Hemodynamically unstable polytrauma patients.
- •Patients who are ASA 4 and above.
结局指标
主要结局
To assess and compare the analgesic efficacy of USG guided pericapsular nerve group (PENG) block with fascia iliaca compartment block (FICB) using VAS score during positioning of hip fracture patients within 30 minutes before neuraxial block.
时间窗: At 10, 20, 30 minutes
次要结局
- To compare the quality of positioning in the two groups for neuraxial block which will be assessed by the anaesthesiologist’s satisfaction and spinal angle.(At 30 minute)
- To compare the patient’s acceptance of the technique.(At 24 hour)
- To study any complications associated with the block.(24 hour monitoring)
- To compare the postoperative 24-hour analgesic requirement in the two groups.