Comparison of superficial cervical plexus block and intravenous morphine for analgesia in tympanomastoid surgeries: Randomised double blind control trial.
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
- Post operative pain will be assessed using VAS score at extubation and later at 1hr, 3hrs , 6hrs, 12 hrs and 24 hrs post surgery.
研究概览
简要总结
Aim of the study:
To assess the effectiveness of superficial cervical plexusblock in providing post operative analgesia for tympanomastoid surgeries.
Objectives of the study:
1. Primary objective:
To compare superficial cervical plexus block V/S intravenous morphine inproviding post operative analgesia by visual analog score(VAS) fortympanomastiod surgeries.
2. Secondary objectives:
A. Comparision of post operative nauseaand vomiting in patients receiving superficial cervical plexus block and inthose receiving morphine for analgesia.
B. Comparison of hemodynamic parameterslike heart rate(HR) and blood pressure(BP) in superficial cervical plexus blockgroup and morphine group.
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
- •ASA 1 and 2 patients of either sex, undergoing tympanomastoid surgery.
- •Age 18 to 60 years.
排除标准
- •Patients undergoing redo surgeries 2.Patients having associated associated facial nerve palcies and skull base osteomyelitis and meningitis.
- •3.PONV, motion sickness, migraine, history of seizures, malignancy, allergy to drugs used in the study.
- •4.Pregnancy and lactating mothers.
结局指标
主要结局
Post operative pain will be assessed using VAS score at extubation and later at 1hr, 3hrs , 6hrs, 12 hrs and 24 hrs post surgery.
时间窗: Postoperatively:1hr, 3hrs , 6hrs, 12 hrs and 24 hrs post surgery.
次要结局
- 1.Intra Operative vitals:(BP, PR at incision,and then at 15mins,30 mins, 1hr, 2hr, 3hrs.)