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临床试验/NCT06589284
NCT06589284已完成不适用

Skin Glue Versus Suture for Securing Radial Arterial Lines

CHRISTUS Health2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
2
主要终点
Length of time which the catheter remained in place

研究概览

简要总结

Prior investigators have evaluated the use of 2-octyl cyanoacrylate (glue) as a method to secure a variety of venous catheters including central/peripheral lines. There is a paucity of research evaluating the use of glue for arterial catheters. The investigators conducted a pilot study to test the null hypothesis that there would be no difference in failure rates between radial arterial lines (r-a-line) secured with glue vs. suture.

详细描述

This was a prospective, randomized, controlled, trial for which the investigators enrolled a convenience sample of consenting, non-pregnant, adult patients who received an r-a-line in the ICU or ED at a community-based, teaching hospital. After randomization, lines were secured with either silk 0-0 suture or 2-octyl cyanoacrylate and, then, covered by chlorhexidine gluconate dressing. Patients were followed for duration of line placement and for the occurrence of premature line failure. Categorical data were analyzed by chi-square; continuous data by t-tests.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

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

  • Be at least 18 years of age
  • Require invasive blood pressure monitoring via radial arterial catheter

排除标准

  • Under 18 years of age

结局指标

主要结局

Length of time which the catheter remained in place

时间窗: 12 months

Primary outcomes measured were length of time of which the catheter remained in place and causes of premature failure, if it occurred.

Cause of premature failure (if occurred)

时间窗: 12 months

Primary outcomes measured were length of time of which the catheter remained in place and causes of premature failure, if it occurred.

次要结局

  • Evaluation of patient demographics for line failure(12 months)
  • Evaluation of line placement for line failure(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Richman, MD

Professor and Research Director, Department of Emergency Medicine, CHRISTUS Health/Texas A&M College of Medicine, Residency in Emergency Medicine

CHRISTUS Health

研究点 (2)

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