Probe-based Confocal Laser Endomicroscopy in Critically Ill COVID-19 Patients

  • STATUS
    Recruiting
  • participants needed
    15
  • sponsor
    Federal Research Clinical Center of Federal Medical & Biological Agency, Russia
Updated on 16 February 2024
critical illness
ct scan
pneumonia
chronic obstructive pulmonary disease
covid-19
critically ill
respiratory failure
lung disease

Summary

The study is devoted to the comparative analysis of the data received in patients with COVID-19 lung pathology using the method of probe-based confocal laser endomicroscopy of distal airways and two reference methods: high resolution computed tomography and morphology (in some patients).

Details
Condition Covid 19
Age 18years - 90years
Treatment miniprobe Alveoflex
Clinical Study IdentifierNCT04451889
SponsorFederal Research Clinical Center of Federal Medical & Biological Agency, Russia
Last Modified on16 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Patient Informed Consent
the diagnosis of COVID-19 or one of the following lung diseases: chronic obstructive pulmonary disease, pneumonia, solitary nodule, pulmonary sarcoidosis, idiopathic interstitial pneumonia, hypersensitivity pneumonitis, pulmonary vasculitis, pulmonary eosinophilia, hemochromatosis, histiocytosis X, pulmonary lymphangioleiomyomatosis; alveolar proteinosis, other rare lung disease
high resolution computed tomography scans performed not later than one month before pCLE (for non-COVID-19)
planned or performed histology (for non-COVID-19)
Severe respiratory failure

Exclusion Criteria

pregnancy or breast feeding
lung bleeding
any acute or chronic disease that may be a contraindication to bronchoscopy
any diseases of hematopoietic system
taking part in other clinical trials
Clear my responses

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.