The Transversus Abdominis Plane Block: A Prospective Randomized Clinical Trial Using EXPAREL.
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Postoperative Pain Score
研究概览
简要总结
The purpose of the study is to evaluate the effectiveness of EXPAREL in a transversus abdominis plane block by assessing the demand of postoperative narcotic, length of hospital stay and incidence of postoperative complications.
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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients over the age of 18 years w
- •Elective laparoscopic colorectal resection.
排除标准
- •Patients under 18 years.
- •Patients unable to provide informed consent
- •Patients undergoing emergency surgery.
- •Pregnant women
- •Severe liver or kidney disease (GFR 15-29 ml/min)
研究组 & 干预措施
TAP Block Experal
Patient who randomized to this arm, will be blinded, TAP block will be performed under ultrasound guidance, where 20-30 ml of Exparel will be injected in transversus abdominis plane, bilaterally.
干预措施: Exparel (Drug)
TAP Block Experal
Patient who randomized to this arm, will be blinded, TAP block will be performed under ultrasound guidance, where 20-30 ml of Exparel will be injected in transversus abdominis plane, bilaterally.
干预措施: TAP Block (Procedure)
结局指标
主要结局
Postoperative Pain Score
时间窗: participants will be followed for the duration of hospital stay, an expected average of 4 days
Patient will be evaluate for their post operative pain by nurses using visual analog scale from 0 to 10, zero means no pain, 10 is the worst pain can patient ever experience.
次要结局
- Postoperative Narcotic Use(participants will be followed for the duration of hospital stay, an expected average of 4 days)