Monitoring lung function in ARDS patients using electrical impedance tomography

Early Prone Positioning Monitored by Electrical Impedance Tomography in Patients With Acute Respiratory Distress Syndrome

Not applicable Interventional Beijing Chao Yang Hospital · NCT05822869

This study tests if using a special monitoring tool can help doctors adjust breathing machines for patients with ARDS to improve their oxygen levels while keeping their lungs safe.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment60 (estimated)
Ages18 Years and up
SexAll
SponsorBeijing Chao Yang Hospital Academic / other
Locations1 site (Beijing, Beijing Municipality)
Trial IDNCT05822869 on ClinicalTrials.gov

What this trial studies

This clinical trial investigates the use of electrical impedance tomography (EIT) to guide mechanical ventilation strategies in patients with Acute Respiratory Distress Syndrome (ARDS). The study aims to improve oxygenation by utilizing prone position ventilation, which enhances ventilation to the dorsal lung regions. Participants will be monitored using EIT technology to adjust ventilator parameters effectively while maintaining lung-protective ventilation strategies. The trial focuses on patients who have been intubated for less than 36 hours and have specific oxygenation criteria.

Who should consider this trial

Good fit: Ideal candidates for this study are adults aged 18 and older who meet the diagnostic criteria for ARDS and have been intubated for less than 36 hours.

Not a fit: Patients who have contraindications to the prone position or EIT, or those who have received extracorporeal membrane oxygenation treatment, may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could significantly improve oxygenation and reduce mortality rates in ARDS patients.

How similar studies have performed: Other studies have shown promising results with prone position ventilation in ARDS, but the use of EIT for monitoring in this context is relatively novel.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age ≥ 18 years old;
2. Meets the diagnostic criteria for ARDS according to the 2012 Berlin definition;
3. Intubation with invasive mechanical ventilation time \< 36 hours;
4. PaO2/FiO2 \< 150mmHg.

Exclusion Criteria:

1. Contraindication to the prone position;
2. Contraindication to the EIT;
3. Patients have received extracorporeal membrane oxygenation treatment.

Where this trial is running

Beijing, Beijing Municipality

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Acute Respiratory Distress Syndromeacute respiratory distress syndrome, prone position, electrical impedance tomography, mechanical ventilation
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.