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Investigating the Effectiveness of Probiotic Supplements in Improving Clinical Symptoms of Allergicrhinitis

Investigating the Effectiveness of Probiotic Supplementaris in Improving Clinical Symptoms of Allergicrhinitis in Children(5 -18 years)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150426021944N8
Enrollment
70
Registered
2026-01-29
Start date
2026-02-04
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Allergic rhinitis. Vasomotor and allergic rhinitis

Interventions

Intervention 1: Intervention group: Participants in this group receive one daily capsule of the probiotic supplement ProKid for four weeks. The supplement contains Lactobacillus acidophilus, Lactobaci

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 18 Years

Inclusion criteria

Inclusion criteria: Children aged 5 to 18 years with allergic rhinitis Presence of clinical symptoms of allergic rhinitis including sneezing, nasal itching, rhinorrhea, or nasal congestion Diagnosis of allergic rhinitis confirmed by an Allergy and Immunology specialist No use of probiotic supplements within 4 weeks prior to study enrollment No use of antibiotics within 4 weeks prior to study enrollment No history of chronic gastrointestinal diseases No history of autoimmune diseases No history of immunodeficiency disorders

Exclusion criteria

Exclusion criteria: Non-compliance with regular consumption of probiotic supplements or placebo Occurrence of severe adverse effects related to probiotic supplementation Modification of the primary allergic rhinitis treatment by the treating physician during the study period

Design outcomes

Primary

MeasureTime frame
Severity of allergic rhinitis clinical symptoms including sneezing, rhinorrhea, nasal itching, and nasal congestion. Timepoint: Measurement at baseline before the intervention and at the end of the fourth week after the intervention. Method of measurement: Total Nasal Symptom Score questionnaire.;Allergy related quality of life in children with allergic rhinitis. Timepoint: Measurement at baseline before the intervention and at the end of the fourth week after the intervention. Method of measurement: Mini Rhinoconjunctivitis Quality of Life Questionnaire.;Total serum Immunoglobulin E level. Timepoint: Measurement before the intervention and at the end of the fourth week after the intervention. Method of measurement: Serum laboratory assay for measurement of total Immunoglobulin E.

Countries

Iran (Islamic Republic of)

Contacts

Public Contact??Dr. Hamid Reza Houshmand

Oroumia University of Medical Sciences

hamidreza.houshmand@gmail.com0098 44 3334592

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026