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Active, not recruitingNCT04702542Updated May 21, 2025

To Develop Methods for the Rehabilitation of Chronic Gastroduodenal Pathology in Children.

An interventional study of Enteral oxygen therapy in Gastritis Chronic, Gastroduodenitis and Peptic Ulcer, sponsored by Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan. Active, not recruiting at 1 site in Uzbekistan. Open to participants aged 6 Years to 15 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-05-21.

Sponsored by Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
320
Allocation
Not applicable
Ages
6 Years to 15 Years
Sex
All
01

Study summary

The object of the study will be children and adolescents from 6 to 15 years old, living in the city of Tashkent and in the Tashkent region. We will study patients with various clinical forms of chronic gastroduodenal pathology (CGDP). The effect of enteral oxygen therapy in the recovery of patients with CGDP due to the positive effect of the active form of oxygen on the hematological system and on the regenerative processes in the gastrointestinal tract will be studied. At the same time, the effect of enteral oxygen therapy on enhancing the effectiveness of eradication therapy during the treatment of carrier Helicobacter pylori due to the neutralization of the products of urea hydrolysis around bacteria under the action of reactive oxygen species will be studied.

Read the detailed description

In recent years, among the non-infectious diseases of children and adolescents, there has been an increase in many nosological forms of pathology of the gastrointestinal tract. Scientific works of recent years show that all over the world much attention is paid to the problem of timely prevention and improvement of chronic diseases of the gastroduodenal zone in children. This is mainly due to the fact that the incidence of diseases of the digestive system among schoolchildren is steadily increasing. In the clinical practice of gastroenterologists, it is often necessary to influence the regeneration processes in the gastroduodenal zone. The object of the study will be children and adolescents from 6 to 15 years old, living in the city of Tashkent and in the Tashkent region. We will study patients with various clinical forms of chronic gastroduodenal pathology (CGDP). The effect of enteral oxygen therapy in the recovery of patients with CGDP due to the positive effect of the active form of oxygen on the hematological system and on the regenerative processes in the gastrointestinal tract will be studied. At the same time, the effect of enteral oxygen therapy on enhancing the effectiveness of eradication therapy during the treatment of carrier Helicobacter pylori due to the neutralization of the products of urea hydrolysis around bacteria under the action of reactive oxygen species will be studied.

02

Conditions studied

  • Gastritis Chronic
  • Gastroduodenitis
  • Peptic Ulcer
  • Duodenal Ulcer

Keywords

  • children
  • duodenal ulcer
  • gastritis
  • gastroduodenitis
  • Helicobacter pylori
  • oxygen therapy
  • rehabilitation
  • peptic ulcer
  • teenagers
03

In context

Gastritis

196 studies on the registry are indexed under Gastritis; 42 are open to participants now.

This study's planned enrollment of 320 is above the median of 200 across 113 interventional studies indexed under Gastritis.

Browse Gastritis studies →

Lead sponsor

Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 15 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • children and adolescents aged 6 to 15 years;
  • children with chronic gastroduodenal pathology: chronic gastritis, chronic gastroduodenitis, chronic duodenitis, gastric and intestinal ulcers of both sexes;
  • children who have the opportunity to visit the clinic.

Exclusion criteria

Exclusion Criteria:

  • children under 6 years old and adolescents over 15 years old;
  • children with chronic diseases of internal organs, except for the gastrointestinal tract;
  • children with psychosomatic and neurological disorders;
  • children in hospital;
  • children with endocrine diseases;
  • children who are allergic to eggs;
  • children with blood diseases;
  • children with cancer.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
320 participants (estimated)

Study arms

  • Experimental
    Enteral oxygen therapy for the improvement of children with chronic gastroduodenal pathology.

    Enteral oxygen therapy is prescribed for children with chronic gastroduodenal pathology during the recovery period, after inpatient treatment, for 14 days, every day, in the form of an oxygen cocktail. An oxygen cocktail is prepared on the basis of a pharmaceutical product using herbal ingredients. The patient takes a 200 ml oxygen cocktail. using a small spoon, during the daytime.

    Drug: Enteral oxygen therapy

Interventions

  • DrugEnteral oxygen therapy

    Enteral oxygen therapy during the rehabilitation period of patients with CGDP.

    Also known as: Standard recreational activities for children after inpatient treatment.

06

What researchers measure

Primary outcomes

  1. Initial clinical examination of children and adolescents at risk of CGDP.

    A clinical examination of patients will be carried out, consisting of: identification of complaints - epigastric pain, dyspeptic symptoms - vomiting, panos, constipation, loss of appetite (oral questioning based on standard questions and scale HBSC (Health Behaviour in School-aged Children, A.King, 1996); collection of data on the presence in the family of a patient with this disease (oral survey based on standard questions); general examination of the patient - the presence of abdominal pain syndrome, stiffness of the abdominal muscles, intestinal distention (palpation, percussion, auscultation).

    Time frame: 2 weeks

  2. Identification of Helicobacter pylori infection.

    The study for Helicobacter pylori (HP) infection will be based on the qualitative determination of the pathogen by two mutually unrelated methods: using a breath test (HELIK® test system with an indicator tube) and an immunochromatographic fecal sample for the presence of occult blood (erythrocyte cells).The interpretation of the test is either "positive" or "negative". The patient will be considered HP infected if both tests are positive.

    Time frame: 2 weeks

  3. Esofibrogastroduodenoscopy at the start of the study

    Esofibrogastroduodenoscopy is carried out with an assessment of the endoscopic picture of the visible mucous membranes of the stomach and duodenum according to the criteria of the generally accepted Sydney classification (1990, with a modification of 1996), with a description of the visible mucous organ: the presence of areas of hyperemia, ulcers, atrophy, hypertrophy, scarring (visual description).

    Time frame: 2 weeks

  4. Treatment of identified patients.

    If a disease is detected, the patient will be referred for treatment to a specialized children's hospital (Tashkent), where he will receive appropriate treatment according to generally accepted standards. The effectiveness of treatment will be assessed by the manifestation of clinical symptoms: the presence of complaints - epigastric pain, dyspeptic symptoms - vomiting, panos, constipation, loss of appetite (oral questioning based on standard questions); general examination of the patient - the presence of abdominal pain syndrome, stiffness of the abdominal muscles, intestinal distention (palpation, percussion, auscultation).

    Time frame: 6 weeks

  5. Rehabilitation of patients using enteral oxygen therapy.

    Rehabilitation of children and adolescents with chronic gastroduodenal pathology after inpatient or outpatient treatment using enteral oxygen therapy is carried out. Studies will be conducted on the content in the peripheral blood in patients: hemoglobin (HGB, Hb, g/dL), erythrocytes (RBC, n x 1012/L), the content of hemoglobin in the erythrocyte (MCH, pg/cell), concentration in the erythrocyte of hemoglobin ( MCHC, g/dL). EFGDS is performed with an assessment of the endoscopic picture of the visible mucous membranes of the stomach and duodenum, according to the criteria of the generally accepted Sydney classification (1990, with a modification of 1996), with a description of the visible mucous organ: the presence of areas of hyperemia, ulcers, atrophy, hypertrophy, scarring.

    Time frame: 6 weeks

  6. Esofibrogastroduodenoscopy after rehabilitation.

    After rehabilitation measures using enteral oxygen therapy, repeated esofibrogastroduodenoscopy (EFGDS) will be performed. EFGDS is carried out with an assessment of the endoscopic picture of the visible mucous membranes of the stomach and duodenum according to the criteria of the generally accepted Sydney classification (1990, with a modification of 1996), with a description of the visible mucous organ: the presence of areas of hyperemia, ulcers, atrophy, hypertrophy, scarring (visual description).

    Time frame: 2 weeks

Secondary outcomes

  1. Statistical data processing.

    Statistical data processing will be carried out using Microsoft Excel 7.0 for Windows-XP, with the definition of the arithmetic mean (M) and standard deviation (s). When characterizing the statistical significance of the differences, the Student's t-test was used, with the determination of the limit of the confidence interval based on the Student's distribution table. The results will be assessed as statistically significant at a probability level of P \<0.05. Comparison is made between groups of patients receiving enteral oxygen therapy and those not receiving.

    Time frame: 8 weeks

07

Study locations

1 site
  • Tashkent Pediatric Medical Institute
    Tashkent, 100140, Uzbekistan
08

References and documents

Individual participant data

Plan to share: No — Joint study of the regenerative properties of oxygen in chronic pathology of the gastrointestinal tract.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04702542
Lead sponsor
Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan
Responsible party
Turdieva Shokhida Tolkunovna, MD (МD, associate professor of the Department "Outpatient care", Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan) — Principal investigator
First posted
Jan 11, 2021
Start date
Apr 30, 2022
Primary completion
Dec 30, 2025 (estimated)
Completion
Dec 30, 2028 (estimated)
Last update
May 21, 2025

Study contacts

Shokhida Turdieva, MD
study director · Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2025. You cannot join it, but the record below documents what was studied.

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