Efficacy of Preoperative Lidocaine Spray and Local Aensthetics-soaked Nasal Packings on Postoperative Pain After Nasal Closed Reduction
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 33
- 试验地点
- 1
- 主要终点
- postoperative pain in recovery room
研究概览
简要总结
This study is perfored to investigate the efficacy of preoperative lidocaine spray and lidocaine-bupivacaine mixture-soaked nasal packing for acute postoperative pain after nasal closed reduction surgery.
详细描述
To investigate the treatment of postoperative pain after nasal closed reduction surgery, we plan to investigate the effect of preoperative lidocaine spray and lidocaine-bupivacaine mixture-soaked nasal packing for the patinets undergoing nasal closed reduction under general aensthesia, compaing to the control group (normal saline spray and normal saline-soaked nasal packing).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •patients scheduled to receive nasal reduction surgery under general aensthesia
排除标准
- •concomitant disorders (eg. facial bone fractures) concomitant surgery (eg. septoplasty)
研究组 & 干预措施
local anesthetic group
local aensthetic group receive preopetaive lidocaine spray and lidocaine-bupivacine mixture-soaked nasal pacing after nasal reduction surgery
干预措施: Lidocaine (Drug)
control group
control group receive preoperative normal saline spray and normal saline-soaked nasal packing after nasal reduction surgery
干预措施: Lidocaine (Drug)
结局指标
主要结局
postoperative pain in recovery room
时间窗: immediately after surgery
Using VAS, postoperative pain is measured.
次要结局
- rescue analgesics in recovery room(1 hr after surgery)
研究者
Young Eun Moon
Associate professor
The Catholic University of Korea
