- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05090644
Program for the Introduction Into Clinical Practice of the Principles of Personalized and Preventive Medicine Based on the Isolation of Gene Polymorphism in Schizophrenia in People of the Kazakh Ethnic Group
March 13, 2023 updated by: Ildar Fakhradiyev, Asfendiyarov Kazakh National Medical University
Preventive and Personalized Medicine (2021-2023)
This is a GWAS study that aims to identify possible candidate genes associate to schizophrenia by exploring single nucleotide polymorphism (SNP) in a group of schizophrenia, in the Kazakh population.
The investigators hypothesize that the careful phenotyping of the subject sand matching with increase the power to find SNP significantly associated with schizophrenia
Study Overview
Detailed Description
A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases.
The method involves scanning the genomes from many different people and looking for genetic markers that can be used to predict the presence of a disease.
Once such genetic markers are identified, they can be used to understand how genes contribute to the disease and develop better prevention and treatment strategies.
Study Type
Observational
Enrollment (Actual)
700
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, 050000
- Republican Scientific and Practical Center for Mental Health
-
-
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 to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Kazakh population
Description
Inclusion Criteria:
- persons of Kazakh nationality having this ethnicity in the 3rd generation
- age from 18 to 65 years old;
- the dispensary in a psychiatric institution at the place of residence with a diagnosis of "Paranoid schizophrenia";
- the duration of the disease is at least 1 year (from the moment of taking under dispensary supervision):
- absence of severe and chronic somatic diseases;
- absence of severe and chronic neurological diseases;
- absence of comorbid drug addiction pathology;
- signed informed consent to conduct this study
Exclusion Criteria:
- persons of non-Kazakh nationality and Kazakh nationality, not confirmed until the 3rd generation
- age less than 18 years old and over 65 years old;
- those who are on dispensary registration in a psychiatric institution at the place of residence with a diagnosis not related to ICD-10 under the heading F20.0 "Paranoid schizophrenia";
- having a disease duration of less than 1 year (from the moment of taking under dispensary supervision):
- having severe and chronic somatic diseases;
- having severe and chronic neurological diseases;
- having comorbid narcological pathology;
- not signed informed consent to conduct this study
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 |
Intervention / Treatment |
|---|---|
|
Experimental group:
Patients with schizophrenia
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GWAS
|
|
Control group
Patients without schizophrenia
|
GWAS
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of SNPs associated with schizophrenia
Time Frame: 1 year
|
Using GWAS to identify candidate genes associate with schizophrenia
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Kuanysh Altynbekov, PhD, Republican Scientific and Practical Center for Mental Health
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)
March 30, 2022
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 25, 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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1203 (Other Grant/Funding Number: VA Catalyst)
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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