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Comparisons of Two Airway Clearance Techniques

Comparison of Two Airway Clearance Techniques by Electrical Impedance Tomography- a Parallel Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06032871
Enrollment
30
Registered
2023-09-13
Start date
2023-03-16
Completion date
2023-12-30
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Airway Clearance Impairment

Keywords

Airway clearance technique, Ventilator associated pneumonia, Electrical impedance tomography, High frequency chest wall oscillation, Chest physiotherapy

Brief summary

The goal of this clinical trial is to compare the effectiveness of two airway clearance techniques for patients with ventilator associated pneumonia. The main questions it aim to answer are: * effect of the therapies on volume changes * outcome on sputum clearance Participants will receive airway clearance techniques of * chest physiotherapy * high frequency chest wall oscillation.

Detailed description

Sputum can be accumulated in the airways of intubated patients, resulting in recurrent pneumonia. The airway clearance therapy is often utilized with chest physiotherapy or high frequency chest wall oscillation which has become popular for its easy of use and less time consuming to the healthcare workers. The main questions it aim to answer are on effectiveness of the therapies on lung volume changes and sputum clearance by two airway clearance techniques. With the oscillation of entire chest wall, the investigators hypothesize that the high frequency chest wall oscillation is more effectively clear sputum in the distal airways.

Interventions

Patients receive airway clearance by high frequency chest wall oscillation for 30 minutes twice a day.

PROCEDUREChest physiotherapy

Participants received chest physiotherapy twice a day

Sponsors

Hui-Ling Lin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

The group will be coded and masked to the investigator and the outcome accessor.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with chronic pulmonary disease * Diagnosed with ventilator associated pneumonia * Receive airway clearance therapy

Exclusion criteria

* Head injury, spinal injury * Instable hemodynamics * Intercranial pressure \> 20 cmH2O * Active hemoptysis * Empyema * Eye surgery * Abdominal distension * Chest tube insertion * Active tuberculosis

Design outcomes

Primary

MeasureTime frameDescription
end-expiratory lung impedanceMeasurement before intervention, 30 after, 1 hour and 2 hours after interventionChanges of global of impedance of lungs measure by the electrical impedance tomography

Secondary

MeasureTime frameDescription
Weight of secretionsSputum is collected before intervention, 30 after, 1 hour and 2 hours after interventionSputum amount is weighted.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026