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Investigating the effect of probiotics on the clinical symptoms of children with eosinophilic gastroenteritis

Investigating the effect of probiotics compared to placebo on the clinical symptoms of children with eosinophilic gastroenteritis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240419061527N1
Enrollment
50
Registered
2024-05-23
Start date
2024-05-19
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Eosinophilic gastroenteritis. Eosinophilic gastritis or gastroenteritis

Interventions

Intervention 1: Intervention group: PPI and probiotic recipients (one daily Prokid capsule). Intervention 2: Control group: PPI and placebo.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 15 Years

Inclusion criteria

Inclusion criteria: Definitive diagnosis of eosinophilic gastritis based on the following diagnostic criteria In pathological view =30 Eo/HPF in =5 HPF or =70 Eo/HPF in =3 HPF (stomach) =52 Eo/HPF (duodenum) =56 Eo/HPF (ileum) In endoscopic view: micronodules, erogenous and mucosal hyperemia Parents' consent to participate in the study

Exclusion criteria

Exclusion criteria: Non-compliance with the patient's medication Incompleteness of information Cortone/PPI/antibiotics use Patients with immune deficiency Other eosinophilic diseases such as IBD, celiac disease, parasitic diseases and Crohn's disease Cases of disturbed thyroid tests that require treatment

Design outcomes

Primary

MeasureTime frame
Improving digestive symptoms (abdominal pain, diarrhea, nausea and vomiting, and constipation). Timepoint: At the beginning of the study and 10 weeks after the start of treatment. Method of measurement: Check clinical symptoms by asking the patient and family.;The recovery rate in the endoscopic view (number of micronodules, number of erogenous and mucosal hyperemia). Timepoint: At the beginning of the study and 10 weeks after the start of treatment. Method of measurement: Based on endoscopy and gastroenterologist diagnosis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKambiz Eftekharian

Tehran University of Medical Sciences

k-eftekhari@sina.tums.ac.ir+98 21 6739 5090

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026