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Effect of Shelf-Stable Yogurt Containing Probiotic BBMN68 on Alleviating Perennial Allergic Rhinitis

Effect of Shelf-Stable Yogurt Containing Probiotic BBMN68 on Alleviating Perennial Allergic Rhinitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112235
Enrollment
Unknown
Registered
2025-11-11
Start date
2025-11-17
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Allergic rhinitis

Interventions

Treatment Group 1:Heat-inactivated, high-dose probiotic yogurt stored at room temperature.
Treatment Group 2:Heat-inactivated, low-dose probiotic yogurt stored at room temperature.
placebo group:Probiotic-free room temperature yoghurt

Sponsors

China Agricultural University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 65 years. (2) Presence of at least two of the following clinical symptoms for more than one hour daily without medication: sneezing, rhinorrhea, nasal congestion, or nasal itching. (3) A history of persistent rhinitis for at least one year. (4) A positive skin prick test (Skin Index >= 0.5) or a positive serological specific IgE antibody test (>= 0.35 kU/L) to at least one of the following common allergens: House Dust Mite or Dermatophagoides farinae. (5) Willingness to participate in the trial and provision of signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Diagnosis of an allergic disease other than allergic rhinitis (e.g., atopic dermatitis, asthma). (2) Presence of comorbid upper respiratory tract infection, sinusitis, or nasal polyps. (3) Currently pregnant, lactating, or planning a pregnancy. (4) History of congenital immunodeficiency. (5) Regular consumption of probiotic supplements or lactobacillus-containing dairy products and known milk allergy or lactose intolerance. (6) Use of antihistamines or intranasal corticosteroids within one week prior to enrollment; or use of oral corticosteroids within three months prior to enrollment. (7) A history of allergen immunotherapy or regular use of anti-inflammatory drugs. (8) Having received any vaccination within the three months prior to enrollment. (9) Concurrent participation in another clinical trial and deemed by the investigator to be unsuitable for the trial for any other reason.

Design outcomes

Primary

MeasureTime frame
Total Nasal Symptoms Score;Immunoglobulin E;

Secondary

MeasureTime frame
Rhinitis Control Assessment Test;Eosinophil;Intestinal metabolites;Gut flora;Rhinoconjunctivitis Quality of Life Questionnaire;Immune cells;Inflammatory cytokines;

Countries

China

Contacts

Public ContactJingjing He

China Agricultural University

hejingjing_89@163.com+86 151 2009 2404

Outcome results

None listed

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