Using airway resistance changes to guide suctioning for ventilated patients
Mechanisms of Dynamic Airway Resistance Monitoring and Machine Learning for Assessing Pulmonary Inflammation and Guiding Sputum Suction in Mechanically Ventilated Patients
This study will test whether monitoring airway viscous resistance from ventilator waveforms can help time sputum suctioning for patients on mechanical ventilation with ARDS, AECOPD, or severe pneumonia.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 258 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Affiliated Hospital of Nantong University Academic / other |
| Locations | 3 sites (Bengbu, Anhui and 2 other locations) |
| Trial ID | NCT07375667 on ClinicalTrials.gov |
What this trial studies
The trial continuously derives airway viscous resistance metrics from ventilator waveforms and compares dynamic patterns to conventional suctioning schedules. It correlates changes in viscous resistance with inflammatory biomarkers over time to explore temporal relationships. The team aims to establish reference thresholds for special populations and to validate the feasibility and reliability of resistance-based monitoring. Data will be collected at multiple tertiary hospitals in China and used to inform optimal suctioning timing.
Who should consider this trial
Good fit: Patients on invasive mechanical ventilation for ARDS, acute exacerbation of COPD, or severe pneumonia who meet ICU clinical criteria are the intended participants.
Not a fit: Patients with multiple organ failure or active multi-site bleeding (who are excluded) or those not on mechanical ventilation are unlikely to benefit from the intervention.
Why it matters
Potential benefit: If successful, this approach could reduce pulmonary inflammation and complications by prompting suctioning at more precise times, potentially lowering ventilator-associated pneumonia rates and improving recovery.
How similar studies have performed: Previous work supports that timely suctioning improves outcomes, but using ventilator-derived viscous resistance and machine-learning guidance is a novel approach with limited prior clinical validation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical diagnosis of Acute Respiratory Distress Syndrome (ARDS) * Clinical diagnosis of Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD) * Clinical diagnosis of Severe pneumonia Exclusion Criteria: * Clinical diagnosis of multiple organ failure; * Clinical diagnosis of multiple organ bleeding;
Where this trial is running
Bengbu, Anhui and 2 other locations
- The First Affiliated Hospital of Bengbu Medical University — Bengbu, Anhui, China (Recruiting)
- Peking Union Medical College Hospital — Beijing, Beijing Municipality, China (Recruiting)
- the Second Affiliated Hospital of Zhejiang University School of Medicine — Hangzhou, Zhejiang, China (Recruiting)
Study contacts
- Study coordinator: Hong-lei Wu Nursing Department, MS
- Email: wu_honglei@163.com
- Phone: +8613862749927
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.