- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04787588
COVID-19 Infection and Epithelial Cell Markers
March 5, 2021 updated by: Gail Gauvreau, McMaster University
To assess if TSLP expression by airway epithelial cells following COVID-19 infection regulates viral load and disease severity.
Study Overview
Detailed Description
The study aim is to determine the relationship between COVID-19 infection and epithelial cell expression of TSLP.
Two cohorts will be used.
Cohort One will include 100 hospitalized patients with Covid-19, and 100 hospitalized patients without Covid-19.
Cohort 2 will include mild/moderate asthmatics and healthy controls with bio-banked biopsy material used from donors who have previously consented for samples to be used for future research.
Study Type
Observational
Enrollment (Anticipated)
235
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
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Hamilton, Ontario, Canada, L8N 3Z5
- Recruiting
- McMaster Cardio-Respiratory Research Lab
-
Contact:
- Gail Gauvreau, PhD
- Phone Number: 22600 9055259140
- Email: gauvreau@mcmaster.ca
-
Principal Investigator:
- Gail Gauvreau, PhD
-
Contact:
- Phone Number: 22791 9055259140
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Hospitalized patients
Description
Inclusion Criteria:
- Age 18 years and above;
- Able to give informed consent;
- Clinically tested for SARS-CoV-2 (as completed by standard laboratory testing e.g. RT-PCR) and with a positive result and clinical features in keeping with COVID-19 illness. The control group will be patients with a negative RT-PCR COVID-19 test and without any clinical features to suggest COVID-19 illness. In addition, the control group should have NO known or current features of respiratory infection, COPD, asthma, interstitial lung disease, other respiratory inflammatory conditions or lung cancer.
- Able to provide a breath sample (as based on clinical judgement).
Exclusion Criteria:
- none
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
Cohorts and Interventions
Group / Cohort |
|---|
|
Hospitalized patients
100 patients hospitalized with Covid-19, and 100 hospitalized controls without Covid-19
|
|
Mild/Moderate asthma and health controls
20 asthmatic patients, 10 patients with asthma and allergic rhinitis, and 5 healthy controls.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
TSLP expression in nasal epithelium
Time Frame: Through study completion, an average of 1 year
|
Compare the level of TSLP expression in nasal epithelium in patients with and without COVID-19 infection
|
Through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
TSLP expression in endobronchial biopsies
Time Frame: Baseline
|
Epithelial cell expression (protein staining) of TSLP in endobronchial biopsy tissue of asthmatic patients versus normal controls.
|
Baseline
|
|
IL-33 expression in endobronchial biopsies
Time Frame: Baseline
|
Epithelial cell expression (protein staining) of IL-33 in endobronchial biopsy tissue of asthmatic patients versus normal controls.
|
Baseline
|
|
ACE-2 receptor expression in endobronchial biopsies
Time Frame: Baseline
|
Epithelial cell expression (protein staining) of ACE-2 receptor in endobronchial biopsy tissue of asthmatic patients versus normal controls.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
February 14, 2021
Primary Completion (Anticipated)
December 1, 2021
Study Completion (Anticipated)
February 1, 2022
Study Registration Dates
First Submitted
March 4, 2021
First Submitted That Met QC Criteria
March 5, 2021
First Posted (Actual)
March 8, 2021
Study Record Updates
Last Update Posted (Actual)
March 8, 2021
Last Update Submitted That Met QC Criteria
March 5, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11033-T
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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