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Effect of Ventilator Hyperinflation Combined With Body Positioning on ABG in VAP

Effect of Ventilator Hyperinflation Combined With Body Positioning on Arterial Blood Gases In Patients With Ventilator-Associated Pneumonia : A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07854730
Enrollment
40
Registered
2026-10-02
Start date
2026-10-05
Completion date
2026-11-15
Last updated
2026-10-16

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

Conditions

Ventilator Associated Bacterial Pneumonia (VABP), Critical Illness

Brief summary

This study aims to evaluate the effect of ventilator hyperinflation combined with body positioning on arterial blood gases in patients with ventilator-associated pneumonia. Forty-two mechanically ventilated patients will be randomly assigned into two groups receiving the intervention in either supine or lateral decubitus positions. Arterial blood gases will be assessed over a 6-day intervention period. The findings are expected to provide evidence regarding the optimal positioning strategy to enhance the effectiveness of ventilator hyperinflation in improving gas exchange in critically ill patients.

Interventions

a therapeutic technique used by clinicians (Manual or Ventilator Hyperinflation) to clear secretions and recruit collapsed lung tissue, or an inadvertent complic

a respiratory therapy technique that uses a manual resuscitation bag to deliver larger-than-normal, controlled breaths to clear airway secretions and reopen collapsed lung areas

Sponsors

Al-Zaytoonah University of Jordan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Mechanically ventilated patients ≥ 48 hours * Diagnosed with VAP (clinical + chest X-ray) * Age: 40-60 years * Hemodynamically stable * Unilateral lung involvement

Exclusion criteria

* Bilateral lung disease * Unstable cardiovascular conditions * Contraindications to positioning * Re-intubation cases * Presence of pneumothorax or air leak

Design outcomes

Primary

MeasureTime frameDescription
PaCO2Will be assessed at baseline (day 1) pre the intervention of the 1st session and (day 6) post the intervention of the 12th session.partial pressure of carbon dioxide in arterial blood, measuring how effectively the lungs eliminate carbon dioxide
PaO2Will be assessed at baseline (day 1) pre the intervention of the 1st session and (day 6) post the intervention of the 12th session.partial pressure of oxygen dissolved in arterial blood plasma, measured through an Arterial Blood Gas (ABG) test.
SaO2Will be assessed at baseline (day 1) pre the intervention of the 1st session and (day 6) post the intervention of the 12th session.the percentage of oxygen-saturated hemoglobin relative to total hemoglobin in arterial blood, typically measured via an invasive arterial blood gas (ABG) analysis with normal values ranging from 95% to 99%
PaO2/FiO2 (P/F)Will be assessed at baseline (day 1) pre the intervention of the 1st session and (day 6) post the intervention of the 12th session.a clinical metric used to evaluate oxygenation efficiency and diagnose the severity of acute hypoxemic respiratory failure or Acute Respiratory Distress Syndrome (ARDS).

Secondary

MeasureTime frameDescription
Pulmonary complianceWill be assessed at baseline (day 1) pre the intervention of the 1st session and (day 6) post the intervention of the 12th session.the change in lung volume divided by the change in pressure (Δ V / Δ P). Higher compliance means the lungs stretch easily; lower compliance means they are stiff and harder to inflate

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Oct 17, 2026