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The effect of ? syr in allergic rhinitis patients in the pilot study

Not Applicable
Recruiting
Conditions
allergic rhinitis.
Allergic rhinitis due to pollen
J30.1
Registration Number
IRCT20081024001391N4
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

Allergic rhinitis, both seasonal and permanent (intermittent and continuous)
Having criteria for allergic rhinitis based on the ARIA form

Exclusion Criteria

The presence of chronic diseases such as asthma, diabetes, cancer, as well as trauma and recent nose surgery, and women who are pregnant and breastfeeding.
Taking any chemical and herbal medicine known to be effective on allergic rhinitis
lack of literacy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Gene expression levels of IL-5, IL-17A, interferon gamma, IL-4, IL-10, IL-13. Timepoint: The medicine will be taken for 4 weeks. Blood sampling will be at the beginning of the study and after the end of the medication in the fourth week. Method of measurement: with laboratory tests, respectively 1. Isolation of peripheral blood mononuclear cells (PBMCs); 2. Total RNA extraction; 3. cDNA synthesis; 4. Quantitative Real-Time PCR (qRT-PCR)Open in Google Translate•F.
Secondary Outcome Measures
NameTimeMethod
Drug side effects. Timepoint: Second and fourth week. Method of measurement: Medication side effects questionnaire.
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