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临床试验/NCT06631716
NCT06631716尚未招募不适用

Evaluation of the Effectiveness of Mechanically Assisted Sputum Excretion

Sir Run Run Shaw Hospital0 个研究点目标入组 84 人开始时间: 2024年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
84
主要终点
CT

研究概览

简要总结

Retention of airway secretions is a common clinical problem in patients with mechanical ventilation. Effective removal of airway secretions requires a balance between the production and removal of airway secretions through the mucociliary transport system. Effective removal of airway secretions is the basic measure to maintain airway patency and normal alveolar ventilation and oxygenation. At present, a variety of mechanical assisted expectoration devices have been used to remove airway secretions in critically ill patients, including The MetaNeb® System(MetaNeb), High Frequency Chest Wall Oscillation(HFCWO) and (Cycloid Vibration Therapy)CVT. However, there is still a lack of sufficient evidence to evaluate the clinical efficacy of these three different mechanical assisted expectoration devices in airway management of patients with mechanical ventilation. This study aims to observe the clinical efficacy of three different mechanical assisted sputum evacuation devices in airway management of patients with mechanical ventilation atelectasis, and to provide a basis for optimizing the airway management scheme of patients with mechanical ventilation.

研究设计

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

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

  • ≥18 years old.
  • patients who were diagnosed as obstructed airway secretion clearance and required mechanical sputum evacuation in Sir Run Run Shaw Hospital, Zhejiang University School of Medicine. Among them, patients using CVT were included in the CVT cohort, patients using Metaneb were included in the Metaneb cohort, and patients using high-frequency chest wall oscillation (HFCWO) were included in the high-frequency chest wall oscillation (HFCWO) cohort.
  • voluntarily participated in this study and signed the informed consent. If the subjects were unable to read and sign the informed consent form due to incapacity or other reasons, their guardians were required to act for them during the informed consent process and sign the informed consent form. If the subjects were unable to read the informed consent form (e.g., illiterate subjects), witnesses were required to witness the informed consent process and sign the informed consent.
  • Invasive mechanical ventilation ≥48 hours.
  • Atelectasis was confirmed by chest CT, chest X-ray or lung ultrasound.

排除标准

  • BMI≥40kg/m
  • Severe spinal and thoracic deformity.
  • Known or suspected diaphragmatic dysfunction such as phrenic nerve rupture, neuromuscular disease, etc.
  • untreated tension pneumothorax.
  • Active bleeding in the lung.
  • Severe hemodynamic instability (increased dose of vasoactive drugs within 2 hours or MAP≤65mmHg).
  • Severe other organ dysfunction was expected to result in short-term death (7 days) or palliative treatment.
  • Other reasons considered by the medical team not suitable for treatment.
  • Pregnancy status.

结局指标

主要结局

CT

时间窗: From enrollment to the end of treatment at 5 days

3D Slicer 5.0.3 software was used to import the chest CT data set, which consisted of 1.25mm thick continuous CT slices obtained by a multi-slice spiral CT scanner under a conventional dose protocol (120Kv,150mA, pitch 1.0), and then the ''Lung CT Segment'' extension program was used. The lung regions were segmented by manually marking 13 marker points. After marking, all the lung regions were visually displayed, and then the region range was manually corrected using the tools selected in the ''Segment editor''. The ''Lung CT Analyzer'' extension program was then used to quantify the lung zones of ''hyperventilation'', ''normal ventilation'', ''hypoventilation'', and ''no ventilation'', and the proportion of no ventilation areas was obtained by software analysis.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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