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Improvement of ARDS Ventilation-perfusion Matching by Prone Positioning Assessed by EIT

Improvement of Acute Respiratory Distress Syndrome Ventilation-perfusion Matching by Prone Positioning Assessed by Electrical Impedance Tomography

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05765760
Enrollment
77
Registered
2023-03-13
Start date
2023-04-01
Completion date
2025-05-31
Last updated
2025-06-15

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

Conditions

Acute Respiratory Distress Syndrome, Electrical Impedance Tomography, Prone Position

Brief summary

Acute Respiratory Distress Syndrome (ARDS) is a highly lethal disease with limited treatment options. In recent years, prone position ventilation has been shown to improve the mortality rate and lung injury of ARDS patients by promoting lung recruitment, improving ventilation/perfusion (V/Q) ratio, enhancing respiratory system compliance, promoting sputum drainage, and effectively avoiding overinflation of the dorsal lung. Electrical Impedance Tomography (EIT) technology has been used to evaluate the effect of prone position ventilation on lung V/Q matching, and some studies have confirmed that prone position ventilation can improve lung V/Q matching and oxygenation index. However, previous studies were mostly case reports or small-sample physiological studies that lacked dynamic changes in lung V/Q matching during repeated prone position ventilation. Therefore, this study hypothesizes that prone position ventilation can increase lung V/Q matching in ARDS patients, and its improvement is correlated with changes in oxygenation index, invasive ventilation time, and patient prognosis. Repeated prone position ventilation can maintain lung V/Q matching at a higher level, no longer affected by changes in body position, which can accelerate pulmonary function recovery and improve the prognosis of ARDS patients.

Interventions

None listed

Sponsors

Beijing Chao Yang Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

1. Age ≥ 18 years old; 2. meet the diagnostic criteria of Berlin's definition for ARDS; 3. invasive ventilation time \< 48h; 4. PaO2/FiO2 \< 150mmHg.

Exclusion criteria

1. Contraindication to the prone position; 2. Contraindication to the EIT; 3. Hemodynamically unstable; 4. Patients with hypernatremia; 5. Patients have received extracorporeal membrane oxygenation treatment.

Design outcomes

Primary

MeasureTime frameDescription
ICU mortality28 days after enrollmentThe death of patients that occurs during their stay in the ICU

Secondary

MeasureTime frameDescription
Ventilator-free days28 days after enrollmentDays without receiving invasive ventilation at day 28.

Countries

China

Outcome results

None listed

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