Evaluation of the effect of Barley extract in the treatment of chronic urticaria
Phase 2
Recruiting
- Conditions
- urticaria.Urticaria
- Registration Number
- IRCT20210309050643N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 46
Inclusion Criteria
Patients with chronic spontaneous urticaria, aged 18 to 60 years
do not have autoimmune disease or immunodeficiency
wish to participate in the study
Exclusion Criteria
pregnancy
Previous hypersensitivity to the drug or any of the compounds present in the herbal medicinal product
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Detect the effect of barley extract on clinical symptoms of CSU patients. Timepoint: At the beginning of the intervention and 4 weeks after taking the drug. Method of measurement: International Urticaria Registration Questionnaire.
- Secondary Outcome Measures
Name Time Method rticaria clinical symptoms score. Timepoint: At the beginning of the intervention and 4 weeks later. Method of measurement: Urticaria Activity score Questionnaire.;Quality of life of chronic urticaria patients. Timepoint: At the beginning of the intervention and 4 weeks later. Method of measurement: score of Chronic Urticaria Quality of Life questionnaire.;Relapse of patients' clinical symptoms. Timepoint: At the beginning of the intervention and 4 weeks later. Method of measurement: Urticaria Control Test.