Actively Recruiting
Evaluating Two Oscillation Techniques for Lung Clearance in Hypersecretive Mechanically Ventilated Patients: A Randomized Crossover Trial
Led by Capital Medical University · Updated on 2025-01-22
24
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Mechanical ventilation (MV) helps patients who cannot breathe on their own but can cause complications like pneumonia and lung collapse due to mucus buildup in the airways. Patients with tracheostomy tubes often need airway cleaning, but usual suctioning clears only part of the airways. This study compares two airway clearance techniques (ACTs) to find the best way to remove mucus in patients needing long-term MV with tracheostomy tubes. The trial compares Oscillation and Lung Expansion (OLE), which uses a device combining mechanical and medication-based methods to clear mucus, with High-frequency Chest Wall Oscillation (HFCWO), which uses a vibrating vest to help loosen secretions. Patients receive both treatments in a randomized order. The study measures lung air movement and ventilation using electrical impedance tomography (EIT) before and after treatment. Participants are adults aged 18 or older who have airway hypersecretion and have been on mechanical ventilation for more than 48 hours in intensive care. Researchers assess lung function through lung imaging and track lung impedance at several time points after treatment. Safety and effectiveness are monitored during and after the treatments to understand which method better supports lung aeration and ventilation distribution.
CONDITIONS
Official Title
Evaluating the Short-term Efficacy of Two Oscillation Techniques in Hypersecretive Mechanically Ventilated Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older with airway hypersecretion
- Admitted to the ICU
- Requiring mechanical ventilation for more than 48 hours
You will not qualify if you...
- Malignant arrhythmia
- Acute myocardial ischemia
- Pneumothorax, pulmonary bulla, barotrauma, or other lung diseases
- Hemorrhagic disease or coagulation problems causing bleeding
- Skin trauma on the chest
- Pulmonary embolism
- Having a permanent or temporary pacemaker
- Untreated spinal or rib fractures
- Any condition the researchers consider unsuitable for the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beijing Rehabilitation Hospital
Beijing, China
Actively Recruiting
Research Team
J
Jingyi Ge
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here