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临床试验/NCT03202576
NCT03202576已完成不适用

Nasogastric Tube Securement: Comparison of Standard Practice Versus Nasal Bridle for Pediatric Hospitalized Patients

University of Colorado, Denver0 个研究点目标入组 43 人开始时间: 2016年10月1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
43
主要终点
Tube dislodgment

研究概览

简要总结

This study evaluates the use of tape to secure nasogastric tubes compared to securement with a nasal bridle device.

详细描述

Patients who need to have a tube placed through their nose and into their stomach for medical treatments will sometimes have it accidentally removed. A nasal bridle is a device where a magnetic is used to attach a small piece of cloth tape that loops around the nasal septum bone and secures to the nasal gastric tube to prevent it from being pulled out accidentally.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
1 Day 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Admitted to Children's Hospital Colorado to:
  • 6th floor surgical inpatient unit, or
  • 8th floor medical inpatient unit, or
  • Heart Institute (Cardiac Intensive Care Unit or Cardiac Progressive Care Unit), or
  • Interventional Radiology.
  • Require a nasogastric or transpyloric tube (Corpak tube or clear feeding tube) for feeding or bowel cleanout.
  • Predicted length of use is at least 48 hours.
  • Newborn up to 21 years of age
  • Have a completed consent for enrollment into the study.

排除标准

  • Burn patients because standard for placement is the nasal bridle;
  • Patients with contraindications for bridle placement , such as
  • mechanical obstruction of the nasal airway
  • facial or nasal fractures
  • fracture of the anterior part of the cranium, or basilar skull fractures
  • Any tubes placed for decompression (i.e. Salem Sump tubes)
  • Nasally intubated, or
  • With CPAP/BiPAP.

结局指标

主要结局

Tube dislodgment

时间窗: Up to 4 weeks

Compare the rate/percent of nasogastric tube dislodgement utilizing standard tube securement practice vs. nasal bridle (micro bridle) tube securement device in pediatric hospitalized patients.

次要结局

  • Restraint use(Up to 4 weeks)
  • Radiation exposure(Up to 4 weeks)
  • Device usability(Up to 4 weeks)
  • Skin integrity(Up to 4 weeks)
  • Cost(Up to 4 weeks)
  • Patient/Caregiver Satisfaction(Up to 4 weeks)

研究者

申办方类型
Other
责任方
Sponsor

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