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Mechanisms of Dynamic Airway Resistance Monitoring and Machine Learning for Assessing Pulmonary Inflammation and Guiding Sputum Suction in Mechanically Ventilated Patients
Led by Affiliated Hospital of Nantong University · Updated on 2026-01-29
258
Participants Needed
3
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the use of dynamic airway viscous resistance monitoring combined with machine learning to guide sputum suction timing in patients who require mechanical ventilation. The study aims to validate this monitoring method, explore its relationship with inflammatory biomarkers, and provide evidence for selecting the best time to perform suctioning, which may impact the progression of lung inflammation. This research is important because current suctioning decisions mainly rely on physician experience and lack scientific data. Participants are randomly assigned to one of two groups. One group will have their airway viscous resistance continuously monitored, and suctioning will be performed when resistance increases by 6 cmH2O or more. The control group will receive suctioning based on usual clinical signs such as rhonchi and increased peak airway pressure. This comparison aims to assess the reliability and clinical value of airway resistance monitoring for guiding suctioning. During the study, researchers will monitor changes in airway viscous resistance before and after suctioning within 30 minutes. They will also evaluate laboratory test abnormalities and perform sputum bacterial cultures within three days. Participants will be assessed regularly to measure the impact on pulmonary inflammation and clinical outcomes. The study lasts until December 2029 and includes adult patients aged 18 to 90 years diagnosed with conditions like ARDS, severe pneumonia, or acute exacerbations of COPD.
CONDITIONS
Brief Title
Dynamic Airway Resistance & ML: Guide Sputum Suction in Ventilated Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of Acute Respiratory Distress Syndrome (ARDS)
- Clinical diagnosis of Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD)
- Clinical diagnosis of Severe pneumonia
- Age between 18 and 90 years
You will not qualify if you...
- Clinical diagnosis of multiple organ failure
- Clinical diagnosis of multiple organ bleeding
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Duration of mechanical ventilation as determined by clinical team
Participants are randomly assigned to either airway resistance-guided sputum suction where suctioning is initiated based on monitored airway viscous resistance increases, or to conventional suctioning based on clinical signs.
Continuous monitoring during mechanical ventilation with sputum suctioning as needed
Duration - Up to 3 days after treatment
Participants are monitored for changes in laboratory tests and sputum bacterial culture after suctioning procedures.
Assessments including laboratory tests and sputum cultures during this period
Trial Site Locations
Total: 3 locations
1
The First Affiliated Hospital of Bengbu Medical University
Bengbu, Anhui, China, 233000
Actively Recruiting
2
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China, 100000
Actively Recruiting
3
the Second Affiliated Hospital of Zhejiang University School of Medicine
Hangzhou, Zhejiang, China, 310009
Actively Recruiting
Research Team
H
Hong-lei Wu Nursing Department, MS
X
xuan Qian Nursing Department, MS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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