- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06392334
Mast Cells and Its Proteases in COPD
April 26, 2024 updated by: Voronezh N.N. Burdenko State Medical Academy
The Role of Mast Cells and Its Proteases in Chronic Obstructive Pulmonary Disease
Mast cells proteases such as chymase and tryptase will be studied in the tissue of small and large airways in COPD patients
Study Overview
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
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: Yanina Shkatova
- Phone Number: 89611875800
- Email: yankashkat@gmail.com
Study Locations
-
-
-
Voronezh, Russian Federation, 394019
- Recruiting
- Voronezh State Medical University
-
Contact:
- Yanina Shkatova
- Phone Number: 9102498731
- Email: yankashkat@gmail.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
Yes
Description
Inclusion Criteria:
- COPD patients
Exclusion Criteria:
Other lung diseases, tumors, pregnancy
-
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Biopsy
Biopsy of lung tissue will be done
|
Biopsy of lung tissue
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of mast cells in COPD lung tissue
Time Frame: up to 10 -12 months
|
Assesment of mast cells in lung tissue in COPD patients
|
up to 10 -12 months
|
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)
January 29, 2019
Primary Completion (Estimated)
August 30, 2025
Study Completion (Estimated)
September 30, 2025
Study Registration Dates
First Submitted
September 22, 2019
First Submitted That Met QC Criteria
April 26, 2024
First Posted (Actual)
April 30, 2024
Study Record Updates
Last Update Posted (Actual)
April 30, 2024
Last Update Submitted That Met QC Criteria
April 26, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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