COMPARISON OF EFFICACY OF ULTRASONOGRAPHY GUIDED ERECTOR SPINAE PLANE BLOCK FOR POSTOPERATIVE ANALGESIA IN PERCUTANEOUS NEPHROLITHOTOMY WITH CONTROL GROUP
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
- to assess the visual analogue score for pain and to determine the time to first rescue analgesia
研究概览
简要总结
The present study is undertaken to determine the efficacy of Ultrasound Guided(USG) Erector Spinae Plane Block used for postoperative pain management among PCNL patients.Patients admitted for Percutaneous Nephrolithotomy who fulfills the inclusion criteria for the study will be randomised using a computer-generated table of random numbers into 2 groups of 30 patients each: Group A received USG guided ESP Block and Group B is control group.Under aseptic precautions,Subarachnoid block will be performed in all patients in L3-L4 space with 3.00ml 0.5% Hyperbaric Bupivacaine.At the end of the surgery,under aseptic precautions, Erector spinae block is given.20 ml of 0.5% Bupivacaine with 8 mg Dexamethasone will be injected. At 1st request, Injection. Paracetomol 1gm IV will be given and continued every 8th hourly thereafter. For rescue analgesia(when VAS>3), Tramadol 1mg/kg will be given.VAS score will be assessed and recorded at 0hrs,2hrs,4hrs,8hrs,12hrs and 24hrs. The time to first rescue analgesia and the total analgesic consumption in 24hrs will be recorded.Statistical analysis will be entered in MS-EXCEL sheet and analysis will be done using Statistical Package for Social Science(SPSS) version 21. Descriptive and inferential statistics will be used for the results . P value of< 0.05 will be considered to be statistically significant
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 80.00 Year(s)（—）
- 性别
- All
入选标准
- •American society of anaesthesiology grade 1&2 Patients posted for unilateral PCNL.
排除标准
- •Patients not willing to participate in the study.
- •Patients with known allergies to study drug.
- •Contraindications for the subarachnoid block.
结局指标
主要结局
to assess the visual analogue score for pain and to determine the time to first rescue analgesia
时间窗: At baseline,2hrs,4hrs,8hrs,12hrs and 24 hours and to determine the time to first rescue analgesia and compare between both groups.
次要结局
- to determine the total analgesic consumption(24hours)
研究者
DR VAISHALI SAJJAN
Sapthagiri Institute Of Medical Sciences and Research Center