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Completed

NCT Number: NCT05765760

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Beijing Chao-Yang Hospital

Beijing, Beijing Municipality, 100020, China

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Contraindication to the prone position;
  • Contraindication to the EIT;
  • Hemodynamically unstable;
  • Patients with hypernatremia;
  • Patients have received extracorporeal membrane oxygenation treatment.

Treatment and study plan

Primary outcomes

  1. ICU mortality

    Time frame: 28 days after enrollment

    The death of patients that occurs during their stay in the ICU

Secondary outcomes

  1. Ventilator-free days

    Time frame: 28 days after enrollment

    Days without receiving invasive ventilation at day 28.

Sponsors and collaborators

Lead sponsor

Beijing Chao Yang Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Mar 13, 2023
Registry last updated
Jun 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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