Prone Position Assessed by 3D EIT

January 23, 2026 updated by: Peking Union Medical College Hospital

Prone Position Assessment by 3D EIT in ARDS Patients

To investigate global and regional changes in lung ventilation and perfusion induced by prone position in ARDS patients assessed by 3D-EIT. And to investigate the difference between 2D-EIT and 3D-EIT in prone position monitoring.

Study Overview

Study Type

Observational

Enrollment (Estimated)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100730
        • Recruiting
        • Department of Critical Care Medicine, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Patients with ARDS on mechanical ventilation

Description

Inclusion Criteria:

  • patients on mechanical ventilation.
  • Diagnosis of ARDS was based on the Berlin definition
  • Patients in need of prone position because of clinical condition

Exclusion Criteria:

  • Under 18 years of age.
  • Pregnant women;
  • Ribcage malformation
  • Any contraindication to the use of EIT (e.g. automatic implantable cardioverter defibrillator, and implantable pumps).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Regional ventilation monitored by EIT
Time Frame: 5-10minutes
Using EIT to monitor the regional ventilation during supine and prone position, to monitor the ventilation distribution change.
5-10minutes
Regional perfusion monitored by EIT
Time Frame: 5-10minutes
Using EIT to monitor the regional perfusion during supine and prone position, to monitor the ventilation distribution change.
5-10minutes
V/Q monitored by EIT
Time Frame: 5-10minutes
Ventilation and perfusion monitored by EIT in supine and prone position. To evaluate the V/Q match, deadspace and shunt lung region.
5-10minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Respiratory system compliance
Time Frame: 1 day
Monitor the respiratory system compliance during supine and prone position
1 day
SpO2
Time Frame: 1 day
Monitor the SpO2 during supine and prone position
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 31, 2024

Primary Completion (Estimated)

October 31, 2026

Study Completion (Estimated)

December 30, 2026

Study Registration Dates

First Submitted

November 14, 2024

First Submitted That Met QC Criteria

July 17, 2025

First Posted (Actual)

July 24, 2025

Study Record Updates

Last Update Posted (Actual)

January 26, 2026

Last Update Submitted That Met QC Criteria

January 23, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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