Visualizing Regional Lung Ventilation in Patients With Postacute-COVID-19
ViReVentPoCov
Visualisation of Changes in Regional Ventilation in Dyspnoeic Postacute COVID-19 Patients: A Case-control Study Using Electrical Impedance Tomography (EIT)
1 other identifier
observational
150
1 country
1
Brief Summary
There is a lack of data of spontaneous breathing patients with post-COVID-19 syndrome (PCS) examined by Electrical impedance tomography (EIT). We compare 100 patients with PCS with 50 healthy probands.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2022
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 14, 2022
CompletedFirst Submitted
Initial submission to the registry
June 29, 2022
CompletedFirst Posted
Study publicly available on registry
July 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 19, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 28, 2025
CompletedSeptember 25, 2025
September 1, 2025
1 year
June 29, 2022
September 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
pathogenic changes in regional lung ventilation
pathogenic changes in regional lung ventilation considered
until July 2022
Study Arms (2)
dyspnoeic patients with post-acute COVID-19 syndrome
100 patients with/without persisting dyspnea after COVID-19 disease were examined by Electric Impedance Tomography (EIT).
control group
50 healthy volunteers with no lung disease were voluntarily examined by Electric Impedance Tomography.
Eligibility Criteria
100 patients with postacute COVID-19 syndrome who present themselves at the outpatient clinic of the University hospital in Jena (JUH) were examined by EIT. 50 lunghealthy volunteers were examined by EIT at JUH.
You may qualify if:
- for control group: no current lung diseases, over 18 years old
- for patients with postacute COVID-19 syndrome: over 18 years, positive SARS-CoV-2-PCR
You may not qualify if:
- heart pacemaker
- epilepsy
- BMI over 50
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jena university hospital
Jena, Thuringia, 07747, Germany
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Jan-Christoph Lewejohann, Dr.med.
Jena University Hospital
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Investigator
Study Record Dates
First Submitted
June 29, 2022
First Posted
July 1, 2022
Study Start
April 14, 2022
Primary Completion
April 19, 2023
Study Completion
August 28, 2025
Last Updated
September 25, 2025
Record last verified: 2025-09