Status:
COMPLETED
Study of the Effectiveness and Safety of Desloratadine (Aerius) Syrup in Children With Hayfever With or Without Asthma (P03472)
Lead Sponsor:
Organon and Co
Conditions:
Rhinitis, Allergic, Seasonal
Asthma
Eligibility:
All Genders
6-12 years
Phase:
PHASE3
Brief Summary
The purpose of this study was to test the effectiveness and safety of desloratadine (Aerius) syrup in children with hayfever with or without asthma. Patients took desloratadine syrup once a day for 28...
Eligibility Criteria
Inclusion
- Children must be \>= 6 to \< 12 years of age of either sex and any race.
- Children's parent(s) or legal representative(s) must demonstrate their willingness to participate in the study and comply with its procedures by signing an informed consent
- Children must be free of any clinically significant disease (other than SAR) that would interfere with study evaluations
- Children's parent(s) or legal representative(s) must understand and be able to adhere to dosing and visit schedules, agree to report concomitant medications and adverse events to the Investigator or designee
- The diagnosis of seasonal allergic rhinitis with or without intermittent asthma will be assessed by:
- Clinical history of sneezing, rhinorrhea (nasal discharge/running nose or post-nasal drip), nasal stuffiness/congestion and nasal itching and non-nasal symptoms (eye symptoms) as itching, burning, tearing and redness, during the previous pollen season
- Ascertained skin prick positivity (or RAST positivity) to one of the following: grasses, parietaria, birch, hazelnut (the skin test has to be performed within the last year)
- Children must be clinically symptomatic with SAR at Visit 1 (day 1): the total (nasal + non nasal) symptoms score must be \>= 8 with a nasal congestion score of \>= 2, and the non-nasal symptoms severity score must be \>= 2
- Asthma symptoms (wheezing, cough, difficulty breathing, chest tightness) will be evaluated at visit 1 (day 1) and graded only for child with concomitant asthma
Exclusion
- Children who have not observed the designated washout periods for any of the prohibited medications
- Children with persistent asthma (mild, moderate or severe) or perennial allergic rhinitis (PAR)
- Children with rhinitis medicamentosa
- Children who have had an upper respiratory tract or sinus infection that required antibiotic therapy within 14 days prior to Visit 1 (day 1), or children who have had a viral upper respiratory infection within 7 days prior to Visit 1 (day 1)
- Children who have nasal structural abnormalities, including nasal polyps and marked septal deviation, that significantly interfere with nasal airflow
- Children who, in the opinion of the Investigator, are dependent upon nasal, oral or ocular decongestants, nasal topical antihistamines, or nasal steroids
- Children with a history of hypersensitivity to desloratadine or any of its excipients
- Children who have any current clinically significant metabolic, cardiovascular, hepatic, renal, immunologic, neurologic, hematologic, gastrointestinal, cerebrovascular or respiratory disease, or any other disorder which, in the judgment of the Investigator, may interfere with the study evaluations or affect subject safety
- A known lack of response to H1-antihistamines
Key Trial Info
Start Date :
May 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2003
Estimated Enrollment :
54 Patients enrolled
Trial Details
Trial ID
NCT00805324
Start Date
May 1 2003
End Date
August 1 2003
Last Update
February 16 2022
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