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临床试验/NCT03520582
NCT03520582终止不适用

Placement of Novel Endoscopic Enteral Feeding Tube - A Feasibility Study

Société des Produits Nestlé (SPN)1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2017年11月6日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
12
试验地点
1
主要终点
Success rate of postpyloric placement, time to reach intragastric and postpyloric position, ease of insertion, handling and image quality.

研究概览

简要总结

The aim of this study is to evaluate the technical feasibility of the new tube placement technology in healthy volunteers and, if proven feasible, in critically ill patients requiring placement of a feeding tube.

详细描述

Enteral feeding is the preferred route of nutrient delivery in hospitalized patients who cannot eat sufficiently. Placement of enteral feeding tubes carries a risk of misplacement especially in patients who are unable to fully collaborate during the tube placement due to neurological impairment and/or the presence of an artificial airway. The misplacement of a feeding tube in the airways has a high risk of severe complications, including pneumonia, mechanical damage of airways and the lung, and death. The verification of correct tube placement can be done using radiography, or interventions aimed at confirming the location of the tube tip by aspiration of gastric contents, and by auscultation during injection of air.

Approximately 20-25 % of patients treated in intensive care units are likely to need placement of a feeding tube, while undergoing mechanical ventilation and having an artificial airway. This high risk patient group would benefit from technologies allowing direct visualization of tube placement. It is also expected that direct visualization of tube placement will allow confirmation of tube placement and therefore eliminate the need of radiography (radiation).

研究设计

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

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

  • Healthy volunteers
  • Informed Consent as documented by signature (Appendix Informed Consent Form)
  • Age >18 years
  • Age >18 years
  • mechanically ventilated and requiring a placement of a postpyloric feeding tube on clinical indications
  • Informed Consent as documented by signature of relatives

排除标准

  • Healthy volunteers and patients
  • Unrepaired tracheoesophageal fistula
  • history of prior esophageal or gastric surgery
  • esophageal obstruction, stricture, varices or diverticulum
  • esophageal or gastric perforation, gastric or esophageal bleeding
  • recent oropharyngeal surgery
  • cervical spine injury or anomaly
  • Additional exclusion criterion for patients only
  • know severe coagulopathy (defined as thrombocyte count less than 30x10e9/l or International Normalized Ratio (INR) > 3)

结局指标

主要结局

Success rate of postpyloric placement, time to reach intragastric and postpyloric position, ease of insertion, handling and image quality.

时间窗: During Intervention Visit, an average of 24 hours

using a visual analog scale of 1-10, with 1 indicating the best value

次要结局

  • In patients: Necessity of use of additional sedation/analgesia for the procedure in addition to already established sedation in the context of mechanical ventilation.(During Intervention Visit, an average of 24 hours)
  • In patients: Ease of insertion, handling, and image quality assessed using a visual analog scale of 1-10, with 1 indicating the best value.(During Intervention Visit, an average of 24 hours)
  • In patients: Time required to reach gastric and postpyloric placement(During Intervention Visit, an average of 24 hours)
  • Injuries of the oesophagus, stomach or small intestine related to tube placement.(During Intervention Visit, an average of 24 hours)
  • In healthy volunteers, ease of insertion, handling, and image quality assessed(During Intervention Visit, an average of 24 hours)
  • In patients: Usability of specific features - tip steerability, lens rinsing and flushing, air insufflation and fluid extraction.(During Intervention Visit, an average of 24 hours)
  • In healthy volunteers, Usability of specific features - tip steerability, lens rinsing and flushing, air insufflation and fluid extraction(During Intervention Visit, an average of 24 hours)
  • Reflux of stomach contents during tube placement(During Intervention Visit, an average of 24 hours)
  • In healthy volunteers, time required to reach gastric and postpyloric placement(During Intervention Visit, an average of 24 hours)
  • In patients: Subjective global assessment of the intensivist on whether or not the technique is suitable for clinical use in patients.(During Intervention Visit, an average of 24 hours)
  • Bleeding and infection related to tube placement(During Intervention Visit, an average of 24 hours)
  • In patients: Feasibility of the feeding through Veritract tube.(During Intervention Visit, an average of 24 hours)
  • Erroneous placement in larynx and trachea and associated complications (pneumothorax).(During Intervention Visit, an average of 24 hours)

研究者

发起方
Société des Produits Nestlé (SPN)
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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