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临床试验/NCT05056103
NCT05056103终止不适用

Effect of an Automated Secretion Removal Technology, Named TrachFlush, on the Need for Tracheal Suctioning - Protocol for a Study in Intubated and Mechanically Ventilated Intensive Care Unit Patients

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2021年9月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
28
试验地点
1
主要终点
proportion of successful TrachFlush activations from start of the study to complete weaning from the ventilator, or a maximum of 7 days

研究概览

简要总结

SUMMARY Rationale In intubated and mechanically ventilated critically ill patients, removal of airway secretions is typically performed by tracheal suctioning, an intervention that is labor-intensive and very unpleasant for the patient. The current study tests the hypothesis that a novel secretion removal technology named TrachFlush, that pushes airway secretions past and above the cuff of the endotracheal tube, reduces the need for tracheal suctioning.

Objective The primary objective of this study is to evaluate whether use of the TrachFlush reduces the need for tracheal suctioning. In a selection of patients, one secondary objective is to ascertain the exact volume of airway secretions that is pushed past and above the cuff of the endotracheal tube.

Study design Open prospective intervention study. Study population One hundred adult, intubated and mechanically ventilated ICU patients expected to need invasive ventilation > 24 hours.

Intervention The attending nurses activate the TrachFlush when there are secretions present in the larger airways that need to be removed. If this results into a push of airway secretions past and above the cuff of the endotracheal tube, no further action is needed. If unsuccessful, the nurse will perform a standard tracheal suctioning procedure to remove the secretions. In a subset of patients with an endotracheal tube that allows subglottal suctioning, the exact amount of airway secretions present above the cuff will be measured each time the TrachFlush is used.

Main study parameters/endpoints The proportion of successful TrachFlush activations from start of the study to complete weaning from the ventilator, or a maximum of 7 days (primary). Secondary endpoints include the total number of TrachFlush activations during the same time window (all patients), and the exact amount of airway secretions pushed past and above the cuff of the endotracheal tube (in patients with a tube allows subglottal suctioning).

Nature and extent of the burden and risks associated with participation, benefit and group relatedness Inappropriate deflation or inflation of the endotracheal cuff by the TrachFlush could cause harm. However, the cuff pressure will be checked regularly, and if necessary corrected, at least every time the TrachFlush has been used. Patients may benefit from the intervention, as the need for tracheal suctioning may reduce.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
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

  • admission to one of the participating ICUs;
  • intubated with an endotracheal tube containing a cuff;
  • receiving invasive mechanical ventilation; and
  • expected to need invasive ventilation beyond the following calendar day at the moment of inclusion.

排除标准

  • age < 18 years;
  • known or suspected tracheal damage, e.g., after inhalation trauma, thorax trauma, or intubation trauma;
  • any condition for which deflation of the endotracheal cuff is deemed detrimental, e.g., in case high airway pressures are needed; and
  • any infection, or colonization with pathogens that require strict single isolation of the patient (cohort isolation is allowed).

研究组 & 干预措施

TrachFlush

Other

干预措施: TrachFlush (Device)

结局指标

主要结局

proportion of successful TrachFlush activations from start of the study to complete weaning from the ventilator, or a maximum of 7 days

时间窗: 7 days

次要结局

  • incidence of hypoxemia related to the TrachFlush activation or tracheal suction(7 days)
  • Incidence of patient agitation related to the TrachFlush activation or tracheal suctions(7 days)
  • total number of TrachFlush activations during the same time window (all patients)(7 days)
  • The volume of subglottal secretions with each TrachFlush intervention (in a patients with an endotracheal tube in place that allows subglottic suctioning).(7days)
  • Incidence of hypotension related to the TrachFlush activation or tracheal suction(7 days)

研究者

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

Prof. Dr. Marcus J. Schultz

Prof.

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (1)

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