Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
ID07375667

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

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Clinical diagnosis of multiple organ failure
  • Clinical diagnosis of multiple organ bleeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Follow-up

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

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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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