Seasonal Allergic Rhinitis
Conditions
Keywords
Rhinitis, Allergic, Seasonal, Hay Fever, Pollen Allergy, Pollinosis, Rhinoconjunctivitis, Sneezing, Nasal itching, Nasal Congestion, Rhinorrhea, Ocular itching, Ocular redness, Tearing
Brief summary
The objective of the study was to determine the efficacy and tolerability of 20 mg of Bilastine, compared to Desloratadine and placebo for the treatment of Seasonal Allergic Rhinitis.
Detailed description
Pivotal, double-blind, randomized, placebo-controlled, comparative with desloratadine, parallel group, international, multicenter study.The Primary endpoint was the Change in total reflective score on the scale of symptoms associated with seasonal allergic rhinitis indicated by patients at the baseline assessment and over the 2 weeks of the study. A total of 720 patients with seasonal allergic rhinitis were enrolled. Duration of treatment was 14 days, preceded by one week (7 days) of placebo.
Interventions
DRUGBilastine
20 mg (encapsulated) tablets QD/14 days
DRUGDesloratadine
5 mg (encapsulated) tablets QD/14 days
DRUGPlacebo
(encapsulated) Tablets QD/14 days
Sponsors
Faes Farma, S.A.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
12 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* The study disease was diagnosed on the basis of clinical criteria: Nasal symptoms (presence of nasal blockage, sneezing, nasal itching and rhinorrhea) and non-nasal symptoms (ocular itching, lacrimation, itching of ears and/or palate and ocular redness), as well as the skin prick test performed at the time of selection or within the year prior to entering. * Patients with history of Seasonal Allergic Rhinitis, positive skin prick test and symptoms were included if they were between 12 and 70 years old, gave their informed consent, attended the required visits scheduled and also underwent a complete medical examination..
Exclusion criteria
* Patients were excluded if they had a significant nasal abnormality which could interfere with the aim of the study, acute or chronic sinusitis, asthma or any condition, disease or hypersensitivity that could be harmed. * Patients were not allowed to take forbidden medications or not comply the study requirements. * Patients who were currently participating in or had participated in another clinical trial within the previous three months or were planning to travel outside of the study area during the course of the study were excluded. * Pregnant or breast-feeding women were also excluded. * Women of childbearing potential had a pregnancy test done
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| AUC of TSS | 14 days | The area under curve (AUC) of the total symptom score (TSS) since basal visit to D14 visit according to the patient's assessment. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in TSS. Instantaneous score | 14 days | Change in the total score on symptom scale on D7 and D14 visits versus D0 visit (baseline) according to the patient's assessment (instantaneous score). |
| Change in total nasal symptom score (TNSS) | 14 days | Change in nasal symptom score on symptom scale on D7 and D14 visits versus D0 visit (baseline) according to the patient's and investigator's assessment. |
| Change in total non-nasal symptom score (TNNSS) | 14 days | Change in non-nasal symptom score on symptom scale on D7 and D14 visits versus D0 visit (baseline) according to the patient's and investigator's assessment |
| VAS of discomfort | 14 days | Overall assessment of discomfort caused by allergic rhinitis using a visual analog scale (VAS) on D7 and D14 versus D0. |
| Change in TSS. Reflective symptoms | 14 days | Change in the reflective total score on symptom scale on D14 visit and day7 visit versus D0 visit (baseline) according to the patient´s assessment on the previous 12 hours. |
| Allergic rhinitis (AR) quality of life (QoL) questionnaire | 14 days | Quality of Life change versus baseline. |
| Onset of action | 2 days | Symptoms assessment in the first 48 hours since the beginning of the treatment |
| Safety assessment | 14 days | comparison of the adverse event profiles throughout the course of the study, ECGs and safety blood tests on D0 and D14. |
| CGI | 14 days | Investigator's overall clinical impression (CGI) |
Outcome results
None listed