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Effect of Triamcinolone and Jelfum in reducing the symptoms of allergic rhinitis

Phase 1
Recruiting
Conditions
Allergic Rhinitis.
Other allergic rhinitis
J30.8
Registration Number
IRCT20210915052490N1
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
45
Inclusion Criteria

ARIA Criteria Diagnosis of allergic rhinitis

Exclusion Criteria

History of rhinoplasty
Anatomical disorders of the nose
Persistent asthma
Prolonged use of corticosteroids
Tuberculosis
Diabetes
Chronic systemic diseases
Pregnancy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sneezing. Timepoint: At the beginning of the study (before the intervention) and 7, 14, 21 and 28 days after the intervention. Method of measurement: Based on question from the person (The rate of patient sneezing based on the number of episodes of the patient's daily sneezing).;Runny nose. Timepoint: At the beginning of the study (before the intervention) and 7, 14, 21 and 28 days after the intervention. Method of measurement: Based on a question from the person (number of sheets of tissue paper consumed by the patient per day).;Nasal congestion. Timepoint: At the beginning of the study (before the intervention) and 7, 14, 21 and 28 days after the intervention. Method of measurement: Based on the scores that patient gives to these symptoms from zero to three.;Itchy nose. Timepoint: At the beginning of the study (before the intervention) and 7, 14, 21 and 28 days after the intervention. Method of measurement: Based on the scores that patient gives to these symptoms from zero to three.
Secondary Outcome Measures
NameTimeMethod
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