Comparison of the efficacy and side effects of desloratadine with fexofenadine on allergic rhinitis in patients referred to Masih Daneshvari Hospital
Phase 2
Recruiting
- Conditions
- Allergic rhinitis.Allergic rhinitis due to pollenJ30.1
- Registration Number
- IRCT20160516027929N11
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 65
Inclusion Criteria
Age over 12 years
History of allergic rhinitis or diagnosis at first visit
Written consent to participate in the study
Exclusion Criteria
Sensitivity, allergy or adverse reaction to desloratadine and fexofenadine
Patients who have previously been treated with two or more drugs
pregnancy and breastfeeding
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method General clinical symptoms. Timepoint: Before starting treatment and 10 weeks after starting treatment. Method of measurement: Rhinitis Quality of Life Questionnaire.;The severity of eye symptoms. Timepoint: Rhinitis Quality of Life Questionnaire. Method of measurement: Rhinitis Quality of Life Questionnaire.;Severe itching in the nose. Timepoint: Rhinitis Quality of Life Questionnaire. Method of measurement: Rhinitis Quality of Life Questionnaire.;Sleep disorders. Timepoint: Rhinitis Quality of Life Questionnaire. Method of measurement: Rhinitis Quality of Life Questionnaire.
- Secondary Outcome Measures
Name Time Method Evaluation of the clinical symptoms of allergic rhinitis. Timepoint: Before starting treatment and 10 weeks after starting treatment. Method of measurement: Physical examination.