- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05088512
The Role of Genetic Factors in the Development of Bronchial Asthma in the Kazakh Population
March 13, 2023 updated by: Ildar Fakhradiyev, Asfendiyarov Kazakh National Medical University
Preventive and Personalized Medicine (2021-2023)
To research for a genetic marker of bronchial asthma, a single nucleotide polymorphism (SNP) analysis of DNA obtained from the peripheral blood of patients with bronchial asthma and normal control will be performed.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Unrelated Kazaks subjects who have bronchial asthma were recruited in the current study.
Genotyping for various SNP associated due to the linkage disequilibrium patterns is to be performed.
Genotypes would be statistically compared between patients with bronchial asthma and normal control subjects free of bronchial asthma
Study Type
Observational
Enrollment (Actual)
300
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
-
-
-
Almaty, Kazakhstan, 050020
- Kazakhstan
-
-
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
5 years to 65 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Persons with bronchial asthma confirmed by a doctor
Description
Inclusion Criteria:
- Persons with bronchial asthma confirmed by a doctor;
- The age of the patients is from 5 to 60 years;
- Persons of Kazakh nationality, whose paternal and maternal grandparents are Kazakhs.
- Persons who are able and willing to provide written informed consent;
- Persons capable and willing to comply with the research protocol;
Exclusion Criteria:
- Persons who, in the opinion of the researcher, are mentally or legally incapacitated, which prevents obtaining informed consent;
- Pregnant or lactating women;
- Tuberculosis of any localization in the active phase and in history;
- Severe and decompensated diseases of the liver and kidneys, cardiovascular system;
- Severe and decompensated course of endocrine diseases;
- Autoimmune diseases;
- Systemic diseases;
- Oncological diseases;
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
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Experimental group:
Patients with bronchial asthma
|
SNP analysis of the DNA obtained from peripheral blood sample
|
|
Control group
Patients without bronchial asthma
|
SNP analysis of the DNA obtained from peripheral blood sample
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of SNPs associated with bronchial asthma
Time Frame: 1 year
|
Using SNPsto identify candidate genes associate with bronchial asthma
|
1 year
|
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 23, 2021
Primary Completion (Actual)
January 20, 2023
Study Completion (Actual)
January 20, 2023
Study Registration Dates
First Submitted
September 25, 2021
First Submitted That Met QC Criteria
October 21, 2021
First Posted (Actual)
October 22, 2021
Study Record Updates
Last Update Posted (Actual)
March 14, 2023
Last Update Submitted That Met QC Criteria
March 13, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1207
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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