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临床试验/NCT05863455
NCT05863455已完成不适用

Effect of Mild Sedation and Analgesia on Radial Artery Cannulation in Novice Residents: a Prospective, Randomized Controlled Trial

Affiliated Hospital of Jiaxing University1 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2023年5月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
108
试验地点
1
主要终点
Overall success rate

研究概览

简要总结

The aim of this study is to conduct a prospective, single-center randomized controlled study to investigate the effect of mild midazolam combined with sufentanil on radial artery cannulation in novice operators.

详细描述

outcome: patients discomfort,visual analogue scale,First-attempt success rate,the success rate of radial artery cannulation within 10 minutes, Complication rate

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Patients who required arterial cannulation for continuous blood pressure monitoring
  • Aged >20years
  • ASA physical status of 1-3
  • BMI 18-28kg/m2
  • All patients agreed to participate in this study at the time of recruitment and signed an informed consent form.

排除标准

  • a positive Allen's test
  • infection at the puncture site
  • coagulation disorders; arterial diseases (such as Raynaud's disease or thromboangiitis obliterans)
  • use of vasoactive drugs within 30 minutes before measurement during the study
  • patients with arterial abnormalities and bends; hemorrhagic shock
  • arterial atherosclerosis; radial artery puncture within the past 30 days
  • chronic use of opioid or benzodiazepine drugs
  • and known allergies or adverse reactions to benzodiazepines or opioids.

研究组 & 干预措施

mild sedation and analgesia

Experimental

Intravenous injection of 0.1ug/kg sufentanil and 0.03mg/kg midazolam for sedation and analgesia before radial artery cannulation.

干预措施: mild sedation and analgesia (Drug)

control

Active Comparator

Intravenous injection of an equivalent volume of saline before radial artery cannulation.

干预措施: control (Drug)

结局指标

主要结局

Overall success rate

时间窗: During radial artery cannulation (up to 1 hour)

success rate of puncture and catheter placement within 10 minutes.

次要结局

  • patients discomfort(During radial artery cannulation (up to 1 hour))
  • visual analogue scale(During radial artery cannulation (up to 1 hour))
  • First-attempt success rate(During radial artery cannulation (up to 1 hour))
  • Complication rate(postoperative 1 day and 3 day)

研究者

发起方
Affiliated Hospital of Jiaxing University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Qing-he Zhou

Principal investigator

Affiliated Hospital of Jiaxing University

研究点 (1)

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