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临床试验/NCT04241146
NCT04241146已完成不适用

A Randomized Controlled Trial for Optimal Feeding Tube Placement

The University of Texas Health Science Center at San Antonio2 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2018年1月6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
52
试验地点
2
主要终点
Duration of Time

研究概览

简要总结

A randomized controlled trial comparing current standard blind method to CORTRAK enteral access system (CEAS), an FDA approved electromagnetic device to place enteric tubes.

详细描述

Patient population would include patients in pediatric intensive care unit, pediatric cardiac unit, intermediate medical care unit and pediatric floor who receives postpyloric feeding tube placements. The study team are going to monitor total time and number attempts required for each successful placement, correlation of findings on x-ray versus CEAS, cost-effectiveness of this new equipment with standard blind method and decrease in radiation exposure with CEAS.

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
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patient admitted to pediatric floor, intermediate care unit, pediatric intensive care unit, or congenital care unit requiring post-pyloric feeding tube placement of size eight french or more and not meeting any of exclusion criteria

排除标准

  • Under three kilograms, Open chest wall, Open abdominal wall

结局指标

主要结局

Duration of Time

时间窗: Baseline to End of procedure up to 30 minutes

Time taken for placement of enteral tube

次要结局

  • Number of X-Rays(Baseline to End of procedure up to 30 minutes)

研究者

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

Andrew D. Meyer

Andrew Meyer, MD

The University of Texas Health Science Center at San Antonio

研究点 (2)

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