The Role of Genetic Factors in the Development of Atopic Dermatitis in the Kazakh Population
Preventive and Personalized Medicine (2021-2023)
1 other identifier
observational
600
1 country
1
Brief Summary
This is a GWAS study that aims to identify possible candidate genes associate to atopic dermatitisby exploring single nucleotide polymorphism (SNP) in a group of atopic dermatitis, in the Kazakh population. The investigators hypothesize that the careful phenotyping of the subject sand matching with increase the power to find SNP significantly associate with atopic dermatitis
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 25, 2021
CompletedStudy Start
First participant enrolled
October 23, 2021
CompletedFirst Posted
Study publicly available on registry
October 25, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 20, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
January 20, 2023
CompletedMarch 14, 2023
March 1, 2023
1.2 years
September 25, 2021
March 13, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
number of SNPs associated with atopic dermatitis
Using GWAS to identify candidate genes associate with atopic dermatitis
1 year
Study Arms (2)
Experimental group:
Patients with atopic dermatitis
Control group
Patients without atopic dermatitis
Interventions
Eligibility Criteria
KAZAKH POPULATION
You may qualify if:
- Persons with various forms of a confirmed diagnosis of atopic dermatitis;
- The age of the patients is from 18 to 45+ 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;
You may not qualify if:
- Persons under the age of 18;
- Patients with severe concomitant systemic diseases, including cardiovascular, respiratory, hepatic and renal failure
- Patients with severe infectious processes (sepsis, abscess, hepatitis B and C, HIV)
- Persons with mental illness.
- Persons taking corticosteroid drugs, immunosuppressants within the last month;
- 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;
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kazakhstan
Almaty, 050020, Kazakhstan
Biospecimen
Blood
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gulya Sarybaeva, PhD
Asfendiyarov Kazakh National Medical University
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of the Laboratory of Experimental Medicine
Study Record Dates
First Submitted
September 25, 2021
First Posted
October 25, 2021
Study Start
October 23, 2021
Primary Completion
January 20, 2023
Study Completion
January 20, 2023
Last Updated
March 14, 2023
Record last verified: 2023-03