- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07083973
- Original Trial
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
Status
Recruiting
Intervention / Treatment
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
- Name: Huaiwu He
- Phone Number: 01069152301
- Email: tjmuhhw@163.com
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:
- Yun Long
- Phone Number: 15201518815
- Email: icu_longyun@126.com
-
-
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Prone position by 3D-EIT
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.