跳至主要内容
临床试验/NCT03915301
NCT03915301Unknown不适用

VUSCH/PostOperativePainTreatment1

Pavol Jozef Safarik University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年7月20日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
40
试验地点
1
主要终点
Satisfaction with pain treatment assessed by the numerical rating scale VAS

研究概览

简要总结

Comparison of effect between Erector Spinae plane block and conventional opioid treatment after cardiac surgery

详细描述

Comparison of effect between Erector Spinae plane block and conventional opioid treatment after cardiac surgery. In group "A" will be erector spinae plane block provided in the thoracic part of the body, under ultrasound control. In the group B will be analgesia provided by Pethidine. Numerical pain score will be recorded every 2 hours, also usage of analgetics will be recorded in both groups.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Postoperative state after cardiac surgery, Serious pain NRS 8-10

排除标准

  • disagreement

结局指标

主要结局

Satisfaction with pain treatment assessed by the numerical rating scale VAS

时间窗: 12 hours

Pain assessed by VAS 0-10 score

次要结局

未报告次要终点

研究者

发起方
Pavol Jozef Safarik University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kočan Ladislav

Principal investigator

Pavol Jozef Safarik University

研究点 (1)

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