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Development of Methods for Effective Treatment and Improvement of Common Somatic Diseases in Children

Clinical Characterization of Leading Somatic Pathologies in Pediatric Patients: Optimizing Treatment and Medical Rehabilitation Strategies

Status
Enrolling by invitation
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06267859
Enrollment
600
Registered
2024-02-20
Start date
2023-11-08
Completion date
2034-01-30
Last updated
2026-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Heart Defects, Respiratory Diseases

Keywords

children, adolescents, heart diseases, lung diseases, congenital malformations, acute bronchitis

Brief summary

The goal of the clinical study is to clarify the course of common congenital, infectious, and non-infectious diseases in children living in Uzbekistan, and to develop methods for their treatment and rehabilitation. The main questions it aims to answer: * Analysis of common congenital diseases among children; * Analysis of the most frequently diagnosed bronchopulmonary (acute bronchitis with and without obstruction, congenital pneumonia, acute and chronic pneumonia) and cardiovascular diseases in children; * Based on the results of the primary research, common diseases among children will be identified; * Analysis of existing treatment methods and their effectiveness; * Development of modern methods of treatment and rehabilitation of children.

Detailed description

Children's health is a priority in modern medicine. Some childhood diseases are most often encountered in the practice of pediatricians and family doctors. Children with these diseases need early diagnosis, treatment, and rehabilitation. Patient selection criteria are: * children from birth to 15 years; * children permanently residing in the territory where the clinical examination is carried out; * full-term newborns with congenital pneumonia without severe complications; * children with acute bronchitis with airway obstruction; * children with acute pneumonia without complications; * patients without severe chronic diseases. Exclusion criteria: * Teenagers over 15 years old; * Patients with severe neurological and mental diseases; * Patients with endocrinological diseases; * Patients with long-term chronic somatic diseases; * Children without genetic pathologies. Clinical research methods: * Collection of anamnestic data; * General examination of patients (auscultation, palpation, percussion); * If necessary: consultation with a geneticist and pediatric doctors of various specialties (cardiologist, surgeon, urologist, nephrologist, otolaryngologist, pulmonologist, immunologist, allergist) * Standard laboratory tests (general analysis of blood, urine, feces); * Standard biochemical studies (microelements of blood and enzymes in venous blood); * Instrumental studies: chest X-ray, ultrasound examination of internal organs (chest and abdominal organs), computed tomography (chest and abdominal organs); * Studies of enzymatic activity and protease-anti protease imbalance in children in induced bronchial fluid (TTLA, NE, MMP-8, MMP-9, CatG, CatB, CatD, CatL, AAT, A2M, SLPI, TIMP-1). * Study of immunological status (cellular immunity, according to standard methods); Immunological research methods - flow cytometry, mIU/mL: immunogram - CD3, CD3/4, CD3/8, CD19, CD16/56, CD3/16/56, CD3/HLA-; and others; * Study of antioxidant status (TAS, using the PSR method, mmol/L); * Assessing the quality of life of patients (methods: PedsQLtm 4.0; HBSC, indicator: total score on the screening survey).

Interventions

COMBINATION_PRODUCTThe use of a combination of microelements and vitamins against the background of physiotherapy

If necessary, necessary microelements and vitamins will be added to the treatment process. At the same time, physiotherapeutic procedures will be added at the rehabilitation stage.

Sponsors

Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Masking description

working with children from the "frequently ill children" group

Intervention model description

Identification of children from the group of "frequently ill children"; Development of non-invasive diagnostics for respiratory biofilm in children; Development of enzymatic bronchial cleansing in children.

Eligibility

Sex/Gender
ALL
Age
3 Days to 15 Years
Healthy volunteers
No

Inclusion criteria

* children from birth to 15 years; * children permanently residing in the territory where the clinical examination is carried out; \- children with acute bronchitis; * children included in the group of "frequently ill children"; * patients without severe chronic diseases.

Exclusion criteria

* Teenagers over 15 years old; * Patients with severe neurological and mental diseases; * Patients with endocrinological diseases; * Patients with long-term chronic somatic diseases; * Children without genetic pathologies.

Design outcomes

Primary

MeasureTime frameDescription
Working with archival documentation.one yearMedical and statistical analysis of data from children's medical institutions is carried out to identify common somatic diseases in children from birth to 15 years old associated with impaired immunity. Evaluation criterion: * medical archival documentation of children's clinics in the region; * statistical analysis of archival documentation on the morbidity of children (acute respiratory: acute bronchitis and acute pneumonia; cardiovascular diseases: congenital heart disease, congenital and acquired carditis).
Formation of a group of patients to study immunity and the antioxidant system in venous blood.one yearObjective: Preparations for a clinical trial are underway. Work in progress: * 400 children with diseases of the bronchopulmonary system and congenital heart defects will be selected; * preparation and submission to the Ethics Committee under the Ministry of Health of Uzbekistan of all necessary documentation for the planned clinical trial among children; Evaluation criterion: \- The percentage of detection of acute bronchopulmonary and congenital heart defects in the region of residence (results of medical statistics).
Clinical scientific research.five years.A clinical study of sick children (acute respiratory: acute bronchitis and acute pneumonia; cardiovascular diseases: congenital heart disease, congenital and acquired carditis) is being conducted to determine the presence of immunological and antioxidant blood parameters. Work in progress: * Screening medical examination of children (objective examination, general blood test - ELISA method); * Examination of venous blood for indicators of immune status (extended immunogram: CD3, CD3/4, CD3/8, CD19, and others), method: flow cytometry of venous blood, mIU/mL; * the study of antioxidant status in sick children (Total antioxidant status, method: venous blood PCR, mmol/L); * publication of the research results. Evaluation criterion: * opinion of reviewers and experts in this field (comparison of the results obtained by other scientists - immunological and antioxidant research) * changes in immune and antioxidant status indicators in sick children to healthy peers.
Clinical trial evaluation.three yearsThe development and implementation of clinical recommendations for practicing pediatricians, pediatric pulmonologists, and cardiologists on improving children's health with acute respiratory (acute bronchitis, pneumonia) and cardiovascular (CHD, congenital and acquired carditis) diseases. Work in progress: * development and implementation of clinical recommendations for pediatricians, pediatric pulmonologists, and cardiologists; * assessment of the effectiveness of clinical recommendations based on repeated laboratory tests (immunological (flow cytometry, mIU/mL) and TAS (PCR, mmol/L)), after six months of implementation of the recommendations. Evaluation criterion: * opinion of reviewers and experts - review; * assessing the quality of life of patients (methods: PedsQLtm 4.0; HBSC), indicator: total score on the screening survey; * number of recurrent illnesses and complications, indicator: the number of patients as a percentage.

Countries

Uzbekistan

Contacts

PRINCIPAL_INVESTIGATORShokhida T Turdieva, D.Sc.

Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 4, 2026