Chronic Urticaria. Other urticaria: chronic spontaneous urticaria
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with chronic urticaria with doctor confirmation 12 to 65 years old Male and female Have tendency for entering into study Not using any anti urticaria medications during the past week
Exclusion criteria
Exclusion criteria: Pregnancy & breast-feeding Having severe angioedema Having uncontrolled cardiovascular, respiratory, hematologic, urology, immune system, infectious and diabetes Having sensitivity to antihistamine drugs Having sensitivity to Jujube plant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quantity of hives. Timepoint: First of research, 7,14,21,28,56 days after intervention. Method of measurement: Urticaria Activity Score (UAS) questionnaire.;Level of itch. Timepoint: First of research, 7,14,21,28,56 days after intervention. Method of measurement: Urticaria Activity Score (UAS) questionnaire.;Quality of life. Timepoint: First of research, fourth and eighth weeks of study. Method of measurement: Quality of Life Questionnaire of chronic urticaria CU-Q2oL. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sides effects. Timepoint: Fourth and eighth weeks of the study. Method of measurement: Common Terminology Criteria for Adverse Events v5.0 2017. | — |
Countries
Iran (Islamic Republic of)
Contacts
Iran University of Medical Sciences