Effect of Triamcinolone and Jelfum in reducing the symptoms of allergic rhinitis
Phase 1
Recruiting
- Conditions
- Allergic Rhinitis.Other allergic rhinitisJ30.8
- 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
Name Time Method 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
Name Time Method