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临床试验/NCT03237546
NCT03237546已完成不适用

The Use of Serratus Block for Cardiac Surgery

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2017年7月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
21
试验地点
1
主要终点
Amount of intravenous opiates used during the immediate postoperative period

研究概览

简要总结

The purpose of this randomized, un-blinded study is to determine if serratus blocks or Patient Controlled Analgesia (PCA)-alone (no block) offer patients adequate pain relief. This study will compare two standard of care pain management options and the patients narcotic requirements in the immediate postoperative period.

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
None

入排标准

年龄范围
18 Years 至 100 Years(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 of age undergoing robotic cardiac surgery.

排除标准

  • •Patients who are not candidates for serratus block

研究组 & 干预措施

Serratus blocks

Active Comparator

The serratus plane is interstitial tissue, below the serratus muscle. The injection of bupivacaine numbs the anterior branch of the thoracodorsal nerve. This technique allows for the medication to diffuse along the area of the serratus plane to provide numbing of that area. Upon completion of the block, the patient will be evaluated for extubation and emerged from general anesthesia if appropriate.

干预措施: Anesthetic regimen including SB (Procedure)

PCA-alone (no block)

Active Comparator

All subjects will receive fentanyl intravenous patient controlled anesthesia pumps as part of standard care. The amount of fentanyl self-administered by the patient or given by a clinician during 24 hours following surgery will be compared amongst the two groups.

干预措施: Anesthetic regimen including SB or no block (Procedure)

结局指标

主要结局

Amount of intravenous opiates used during the immediate postoperative period

时间窗: 24 Hours

The primary endpoint of the study will be comparison of the amount of intravenous opiates used during the immediate postoperative period between the 2 groups, the group receiving general anesthesia with the serratus block and the group receiving general anesthesia alone.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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