Health Condition 1: L501- Idiopathic urticaria
Conditions
Interventions
Intervention1: DAILY ADMINISTRATION OF ANTIHISTAMINES: DAILY ADMINISTRATION OF BILASTINE AND LEVOCETIRIZINE FOR 2 MONTH
Control Intervention1: DAILY SINGLE DOSE ANTIHISTAMINE: BILASTINE 20MG FOR ONE G
Sponsors
DrKalaiyarasan
Eligibility
Inclusion criteria
Inclusion criteria: All patients of age >18 years presenting to Dermatology department with CSU who are not on any drug for urticaria for the past one week.
Exclusion criteria
Exclusion criteria: 1. Patients above 65 years. 2. Pregnant and lactating women. 3. Other pruritic disorders like eczema, contact dermatitis, and atopic dermatitis. 4. Patient on drug which cause sedation like antipsychotic drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the efficacy of oral Bilastine 20 mg and Levocetirizine 10 mg in patients with Chronic Spontaneous Urticaria will be assessed by using Urticaria Activity Score (UAS), Urticaria Severity Score (USS), Urticaria control test (UCT), Chronic Urticaria Quality Of Life (CU-Q2OL).Timepoint: mean difference in efficacy of oral Bilastine 20 mg and Levocetirizine 10 mg in patients with Chronic Spontaneous Urticaria will be assessed by using Urticaria Activity Score (UAS), Urticaria Severity Score (USS), Urticaria control test (UCT), Chronic Urticaria Quality Of Life (CU-Q2OL) in day 28 an 56 days | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the degree of somnolence produced by both drugs using Epworth Sleepiness Scale (ESS).Timepoint: Mean difference in Somnolence between two groups at day 28 and 56 days. | — |
Countries
India
Contacts
Public ContactDr Sheela Kuruvila
Pondicherry Institute of Medical Sciences
Outcome results
None listed