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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05095129
Other study ID # 1192
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 23, 2022
Est. completion date January 20, 2023

Study information

Verified date March 2023
Source Asfendiyarov Kazakh National Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to identify genetic determinants of susceptibility to idiopathic scoliosis . It will assist in predicting individual risks of disease progression and would help to clarify pathophysiologic mechanisms of idiopathic scoliosis


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date January 20, 2023
Est. primary completion date January 20, 2023
Accepts healthy volunteers
Gender All
Age group 4 Years to 40 Years
Eligibility Inclusion Criteria: 1. Persons with a doctor-confirmed diagnosis of idiopathic scoliosis; 2. Persons of Kazakh nationality, whose paternal and maternal grandparents are Kazakhs; 3. Hereditary history of scoliosis; 4. Persons who are able and willing to provide written informed consent; Exclusion Criteria: 1. Patients diagnosed with idiopathic scoliosis under 4 and over 40 years of age; 2. Representatives of the Kazakh ethnic group less than 3 generations; 3. No family history of bilateral idiopathic scoliosis; 4. Patients with an acute period of the inflammatory process (laboratory and clinical signs); 5. Persons who, in the opinion of the researcher, are mentally or legally incapacitated, which prevents obtaining informed consent; 6. Pregnant or lactating women; 7. Tuberculosis of any localization in the active phase and in history; 8. Severe and decompensated diseases of the liver and kidneys, cardiovascular system; 9. Severe and decompensated course of endocrine diseases; 10. Autoimmune diseases; 11. Systemic diseases; 12. Oncological diseases;

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
SNP analysis of the DNA
SNP analysis of the DNA obtained from peripheral blood sample

Locations

Country Name City State
Kazakhstan Scientific center of traumatology and orthopedics named after academician Batpenova ND Almaty

Sponsors (1)

Lead Sponsor Collaborator
Asfendiyarov Kazakh National Medical University

Country where clinical trial is conducted

Kazakhstan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Genotyping for the SNP associated with liver cirrhosis Genotype frequency of SNP in the study genes of participants and control participants. 1 year
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