Efficacy of Intercostal Block Versus Pectoral Nerve Block II in Controlling Acute Post-surgical Pain in Thoracoscopic Surgery
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 80
- 试验地点
- 2
- 主要终点
- The use of pain medications after surgery
研究概览
简要总结
The investigators will evaluate the efficacy of two types of pain control blocks in patients going thoracoscopic surgery. Patients will be randomly classified into two groups. In the control group, patients will get intercostal block at the end of the surgery and after then will be treated by the customary postoperative pain control regimen. This group represents the existent treating policy.
In the research group, patients with get PECS II block at the end of the surgery and will get a similar postoperative pain control regimen. The investigators hope to find which pain control block is superior.
详细描述
Thoracic operations are among the most post-operative painful surgeries. Without a doubt, the emergence of the thoracoscopic approaches has decreased pain severity. The classical methods of pain control that is used in the open thoracic procedures are not suitable in the thoracoscopic milieu. As such, pain control methods should be examined. The most accepted methods are those using different anesthetic blocks based on local anesthetic (Bupivacaine), whether in intercostal block or paravertebral one. Today the investigators use intercostal block consistently in thoracospoic procedures.
Recently, the use of the pectoral nerve block (Pecs II) has emerged for different chest wall surgeries, which has proved to be helpful. As a consequence,the investigators want to examine the efficiency of this block in the control of postoperative pain after thoracoscopic procedures.
In this prospective comparative study, patients will be randomly classified into two groups. In the control group, patients will get intercostal block at the end of the surgery and after then will be treated by the customary postoperative pain control regimen. This group represents the existent treating policy.
In the research group, patients with get PECS II block at the end of the surgery and will get a similar postoperative pain control regimen.
The follow up will include checking the pain level in the postoperative days, the extent of the pain relief medication until the discharge, and patient evaluation at the first post-discharge inspection.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (Participant)
盲法说明
Patients will not be informed as to which study group they assigned to. Only the caregivers will have this information.
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
- •Candidate for video assisted thoracoscopic surgery
- •Over 18 years of age
- •No known allergy to Bupivacaine
- •Candidate who can read, understand and sign inform consent
排除标准
- •Candidate had previous surgery at the same side
研究组 & 干预措施
intercostal block
patients will get intercostal block at the end of the surgery, control group
PECS II block
patients with get PECS II block at the end of the surgery, research group
干预措施: PECS II block (Procedure)
结局指标
主要结局
The use of pain medications after surgery
时间窗: from the end of surgery until participant hospital release, assessed up to 4 weeks
The amount of pain medications used by each participant in the post surgical period
次要结局
未报告次要终点
研究者
Dan Levy Faber
Senior thoracic surgeon
Carmel Medical Center
