comparative evaluation of ropivacaine and ropivacaine with dexmedetomidine in axillary brachial plexus block for post operative analgesia
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- To evaluate for the duration of post-operative analgesia
研究概览
简要总结
PATIENTS WERE DIVIDED INTO TWO GROUPS . ONE GROUP WILL BE GIVEN INJ ROPIVACAINE 0.5 % WITH 1 ML OF NORMAL SALINE AND ONE WILL BE GIVEN ROPIVACAINE 0.5% WITH DEXMEDETOMIDINE. ON ARRIVAL IN POST OPERATIVE ROOM , PATIENTS WILL BE ASSESSED FOR THE OCCURENCE OF PAIN ON 11 POINTS VISUAL ANALOG SCALE AND THIS WILL BE CONSIDERED AS 0 HOUR ,THEREAFTER THE OCCURRENCE OF PAIN AND HEMODYNAMIC PARAMETERS WILL BE ASSESSED EVERY 30 MINUTES FOR FIRST 6 HOURS AND THEN EVERY 6 HOURLY FOR UPTO 24 HOURS .
INJECTION DICLOFENAC 75 mg INTAMUSCULAR WILL BE ADMINISTERED AS 1ST RESCUE ANALGESIC , WHEN VAS SCORE WILL BE MORE THAN EQUALS TO 4.
INJECTION TRAMADOL50 mg INTRAMUSCULAR WILL BE ADMINISTERED AS 2ND RESCUE ANALGESIC .THE TIME BETWEEN THE END OF LOCAL NAESTHETC ADMINISTRATION AND 1ST RESCUE ANALGESIC ADMINISTRATION WILL BE RECORDED AS THE DURATION OF ANALGESIA
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 60.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Patients with ASA grade I and II.
- •2.Age group 18- 60 years 3 Patient undergoing upper limb surgery under axillary block.
排除标准
- •1.Patient refusal 2.ASA grade III & IV patients 3.History of allergy or sensitivity to local anaesthetic or study drug
- •Known cardiovascular respiratory disease 5.Known hepato renal disease 6.Neuropsychiatric disorders 7.History of bleeding disorder..
- •8.Day care surgery 9.Pregnancy.
结局指标
主要结局
To evaluate for the duration of post-operative analgesia
时间窗: To evaluate for the duration of post-operative analgesia
次要结局
- 1 .To evaluate the onset of sensory and motor block(2 To compare the complete effect of sensory and motor block)