Single blind randamized control trial comparing injection bupivacaine with dexamethasone versus injection bupivacaine with dexmedetomidine in suprainguinal fascia iliaca block for postoperative pain relief in fracture hip surgery
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
- postoperative pain intensity and duration of analgesia with time of first rescue analgesic requirment.
研究概览
简要总结
Patients posted for proposed study will be diploid in the randomized pattern Total of 40 patients will be divided in 2 groups,20 patients in each group. Group DI: Dexamethasone group will receive 8 mg of Inj .Dexamethasone as adjuvant to Inj. Bupivacaine 0.25%
Group DII: Dexmedetomidine group will receive 50 mcg of Inj.Dexmedetomidine as adjuvant to Inj.Bupivacaine 0.25%.
Study implications:
This study will compare the efficacy of Dexamethasone and Dexmedetomidine as an adjuvant to bupivacaine in Suprainguinal fascia Iliaca block for post-operative analgesia in terms of its duration and Intensity. It also highlights its effect on hemodynamic stability.
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 undergoing hip surgery under spinal anaesthesia ASA Grade I and II.
排除标准
- •Patients not willing to participate in study with due consent.
- •Drug allergy to Dexmedatomidine -Patients on B blocker,Heart block -Patients with Psychiatric disorder -Severe cardio-pulmonary disease -severe hepatic,renal disease -Neuromuscular disease.
结局指标
主要结局
postoperative pain intensity and duration of analgesia with time of first rescue analgesic requirment.
时间窗: time of first rescue analgesic requirment.
次要结局
- haemodynamic parameteres,sedation score,total amount of analgesic requirement in first 24 hours(24 hours postoperative period)
研究者
Dr Megha Sonawane
Department of Anaesthsia