Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05822869

Early PP Monitored by EIT in Patients With ARDS

Led by Beijing Chao Yang Hospital · Updated on 2025-06-17

60

Participants Needed

1

Research Sites

139 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Acute Respiratory Distress Syndrome (ARDS) is a syndrome characterized by respiratory distress and refractory hypoxemia caused by pulmonary and extra-pulmonary factors. Despite improvements in diagnosis and treatment in recent years, the mortality rate of severe ARDS is still around 40%. The distribution of lung lesions in ARDS patients is significantly gravity-dependent. Even with lung-protective ventilation strategies, tidal volume is concentrated in the ventral lung region, leading to ventilator-associated lung injury. Prone position ventilation can increase ventilation to the dorsal lung tissue and improve the ventilation-perfusion ratio, thus improving oxygenation. During prone position ventilation in ARDS patients, lung-protective ventilation strategies should be maintained, but with different respiratory mechanics from the supine position, requiring adjustment of ventilator parameters. Electrical Impedance Tomography (EIT) technology can be used for bedside monitoring of mechanically ventilated patients, providing real-time feedback on the patient's ventilation status and having great potential for clinical applications. Investigators believes that EIT monitoring during prone position ventilation in ARDS patients can individualize lung-protective ventilation strategies, minimize alveolar overdistension and collapse, improve the weaning success rate of invasive ventilation, and ultimately improve patient prognosis.

CONDITIONS

Official Title

Early PP Monitored by EIT in Patients With ARDS

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with ARDS according to the 2012 Berlin definition
  • Intubated and on invasive mechanical ventilation for less than 36 hours
  • PaO2/FiO2 ratio less than 150 mmHg
Not Eligible

You will not qualify if you...

  • Contraindication to the prone position
  • Contraindication to Electrical Impedance Tomography (EIT)
  • Previous treatment with extracorporeal membrane oxygenation (ECMO)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beijing Chao-Yang Hospital

Beijing, Beijing Municipality, China, 100020

Actively Recruiting

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Research Team

Y

Yu Zhao, Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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