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Comparing the Safety and Benefits of Bilastine and Desloratadine in Patients with Chronic spontaneous urticaria.

To compare the safety and efficacy of Bilastine 20 mg versus Desloratadine 5mg in patients of Chronic Spontaneous Urticaria an open label, randomized, parallel-group study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097596
Enrollment
60
Registered
2025-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L501- Idiopathic urticaria

Interventions

Intervention1: Bilastine: Participants will receive Bilastine 20 mg tablet, administered orally once daily, 1 hour before or 2 hours after meals, for a total duration of 42 days. Control Intervention1

Sponsors

Dr Rajendra Prasad Government Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients willing to give informed consent. 2.Consenting adults of either sex between 18-65 years of age with documented history of chronic spontaneous urticaria, without any known inducible factor or definite cause. 3.Currently not on any prophylactic medication in last month. 4.Patients ability to fill a Urticaria activity score. diagnosed with CSU( symptoms for more than or equal to 6 weeks.

Exclusion criteria

Exclusion criteria: Dermatoses including dermographism Physical urticaria Hereditary angioedema, Food and/or drug allergy, Contact urticaria, Collagen vascular diseases, Atopic dermatitis, Systemic autoimmune disorders, Hodgkin s disease, Patients who had taken systemic or topical corticosteroids within 4 weeks, or any other oral antihistamine within 72 hours of randomization visit, Any known cause of urticaria like respiratory/ gastrointestinal infections or parasitic infestation were also excluded, Pregnant or lactating women, Known hypersensitivity to Bilastine or desloratadine, Autoimmune thyroid disorder

Design outcomes

Secondary

MeasureTime frame
NIlTimepoint: NIL

Primary

MeasureTime frame
To compare the efficacy of Bilastine 20 mg versus Desloratadine 5 mg in reducing disease activity, measured by the change in Urticaria Activity Score over 7 days (UAS7) from baseline to Day 42 in patients with chronic spontaneous urticaria.Timepoint: Day 0 - baseline day 14 - first followup day 28 - second followup day 42 - third followup/end of treatment

Countries

India

Contacts

Public ContactDr Yiesh Gathania

Dr. Rajendera Prasad Government Medical college

atalsood7@gmail.com9418063191

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026