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Effectiveness of Probiotic Gummies in Relieving Allergic Rhinitis in Children

Effectiveness of Probiotic Gummies in Relieving Allergic Rhinitis in Children

Recruiting
4-14 years
All
Phase N/A

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Overview

To evaluate the effect of probiotic gummies on serum metabolite levels, clinical efficacy, and regulation of gut microbiota in children with allergic rhinitis compared with placebo.

Eligibility

Inclusion Criteria:

  1. Voluntary, written, signed informed consent to participate in this study;
  2. be able to complete the study in accordance with the requirements of the test protocol;
  3. Age 4-14 years old;
  4. Meet the diagnostic criteria for allergic rhinitis established in the Guidelines for the Diagnosis and Treatment of Allergic Rhinitis in Children (2022 Revised Edition);
  5. Symptoms: 2 or more symptoms: sneezing, watery discharge, nasal itching and nasal congestion and other symptoms last or accumulate for more than 1 hour per day, and may be accompanied by eye symptoms such as itching, watery eyes and red eyes;
  6. Signs: pale and edema of the nasal mucosa, which may be accompanied by watery discharge;

Exclusion Criteria:

  1. Drugs that affect the intestinal flora (including antimicrobial drugs, microecological preparations, intestinal mucosal protectors, Chinese patent medicines, etc.) have been used continuously for more than 1 week within 1 month before screening;
  2. Patients with pulmonary tuberculosis;
  3. Combined with allergic asthma;
  4. Those with nasal polyps or severe nasal septum deviation;
  5. Patients with severe systemic diseases or malignant tumors;
  6. Those with congenital genetic diseases and congenital immunodeficiency diseases;
  7. Those who regularly use probiotics or prebiotics within 6 months before the screening period;
  8. Those with severe digestive tract diseases (including severe diarrhea, inflammatory bowel disease, etc.);
  9. Patients with metabolic syndrome (including obesity, dyslipidemia, hypertension, diabetes, etc.);
  10. Patients with sinusitis, otitis media, or respiratory tract infection;
  11. Those who are allergic to the probiotic-related ingredients used in this trial;
  12. Those who stop taking the test sample or add other drugs in the middle of the test, and the efficacy cannot be judged or the data is incomplete;
  13. Those who take items with similar functions to the test in a short period of time, which affects the judgment of the results;
  14. Subjects who are unable to participate in the test due to their own reasons;
  15. Subjects who are judged by other investigators to be insuitable to participate.

Study details
    Children With Allergic Rhinitis

NCT06885632

Wecare Probiotics Co., Ltd.

14 September 2025

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