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临床试验/NCT03937076
NCT03937076Unknown不适用

Efficacy of Intercostal Block Versus Pectoral Nerve Block II in Controlling Acute Post-surgical Pain in Thoracoscopic Surgery

Carmel Medical Center2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2019年6月1日最近更新:
适应症
干预措施

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

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

No Intervention

patients will get intercostal block at the end of the surgery, control group

PECS II block

Experimental

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

发起方
Carmel Medical Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dan Levy Faber

Senior thoracic surgeon

Carmel Medical Center

研究点 (2)

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