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The Effectiveness of Different Nebulized Solutions on Airway Clearance Function in Patients With Pneumonia

The Effectiveness of Different Nebulized Solutions on Airway Clearance Function in Patients With Pneumonia

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07586345
Enrollment
80
Registered
2026-05-14
Start date
2026-05-01
Completion date
2027-12-31
Last updated
2026-05-14

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

Conditions

Airway Clearance, Pneumonia

Brief summary

Pneumonia is a significant global and national health issue, particularly posing a notable threat to elderly population. Accumulation of sputum in pneumonia patients often results in impaired airway clearance, negatively impacting disease management and recovery. Clinically, nebulization therapy is widely employed to facilitate sputum clearance; however, evidence regarding the comparative effectiveness of different nebulized solution concentrations remains limited and inconsistent. Therefore, this study aims to evaluate and compare the clinical effects of nebulized solutions with various osmotic concentrations (3% hypertonic saline, 0.9% normal saline, 0.45% hypotonic saline, and distilled water) on airway clearance in patients with pneumonia. A randomized, double-blind controlled trial design will be used, recruiting 80 patients with pneumonia from a regional teaching hospital in northern Taiwan. Participants will be randomly assigned into four groups, receiving nebulized therapy four times daily over a period of seven days. This study outcome including the length of hospital stay, venous blood gas analysis, routine sputum examination, and arterial oxygen content. The findings of this the study are anticipated to provide evidence-based recommendations for the clinical application of nebulized solutions with different concentrations, aiming to enhance airway clearance efficiency, improve clinical care outcomes for pneumonia patients, and serve as a practical reference for healthcare professionals.

Interventions

OTHERNebulization therapy

Comparison of different concentrations of saline solutions used for nebulization therapy

Sponsors

Chen, Yao-Hsiang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosed with pneumonia, defined by ICD-10 codes, including: J18: Pneumonia, unspecified organism J180: Bronchopneumonia, unspecified organism J181: Lobar pneumonia, unspecified organism J182: Hypostatic pneumonia, unspecified organism J188: Other pneumonia, unspecified organism J189: Pneumonia, unspecified organism 2. Aged 18-100 years 3. Clinical respiratory score \> 3 4. Patients unable to expectorate sputum spontaneously and requiring assisted suctioning

Exclusion criteria

1. Diagnosis of influenza-associated pneumonia, defined by ICD-10 codes, including: J09X1: Influenza due to identified novel influenza A virus with pneumonia J1001: Influenza due to other identified influenza virus with the same identified influenza viral pneumonia J100: Influenza due to other identified influenza virus with pneumonia 2. Diagnosis of COVID-19 infection, defined by ICD-10 code: U07.1: COVID-19, virus identified 3. History of chronic obstructive pulmonary disease (COPD) (ICD-10 code: J44) 4. History of lung cancer or metastatic cancer involving the lungs 5. Current use of bronchodilators 6. Patients requiring oral suctioning only 7. Oxygen therapy with a flow rate \> 10 L/min 8. Clinical respiratory score \> 8 (Table 2)

Design outcomes

Primary

MeasureTime frameDescription
Vein blood gasMeasurements were performed before the intervention and at 7 days after the intervention.Assessment of venous blood gas values including pH, pCO₂, and HCO₃-.
Sputum routine examinationMeasurements were performed before the intervention and at 7 days after the intervention.Assessment of sputum characteristics and routine laboratory findings.
Arterial oxygen content (CaO₂)Measurements were performed before the intervention and at 7 days after the intervention.Measurement of arterial oxygen content calculated from hemoglobin concentration, oxygen saturation, and partial pressure of oxygen. Unit of Measure: mL O₂/dL blood

Secondary

MeasureTime frameDescription
Blood lactic acid levelMeasurements were performed before the intervention and at 7 days after the intervention.Measurement of serum lactic acid concentration. Unit of Measure: mmol/L

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026