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Clinical Trial Summary

The purpose of the current study is to evaluate the efficacy of administering a multistrain probiotic in adult human subjects suffering from allergic rhinitis and evaluate both symptomatology through validated questionnaires and gut microbiota modification during and after treatment.


Clinical Trial Description

Adult subjects (18-60) with documented allergic rhinitis will be assigned to placebo or probiotic groups and take either placebo or probiotic dietary intervention for 8 weeks. Total nasal symptom score (TNSS), Rhinitis Control Assessment Test (RCAT), Mini Rhinoconjunctivitis Quality of Life Questionnaire (MiniRQLQ) will be compared over 12 weeks between the two treatment groups. In addition, serological markers (Eosinophil count, Total IgE and Eosinophilic cationic protein) and gut microbiota features will be evaluated over a 12 week period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05344352
Study type Interventional
Source Università degli Studi di Ferrara
Contact Giacomo Caio, MD, PhD
Phone +39 0532236823
Email caigmp@unife.it
Status Recruiting
Phase N/A
Start date March 30, 2022
Completion date June 30, 2024

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