Effectiveness of Beclomethasone Dipropionate Nasal Aerosol for Perennial Allergic Rhinitis
Status: | Completed |
---|---|
Conditions: | Allergy |
Therapuetic Areas: | Otolaryngology |
Healthy: | No |
Age Range: | 12 - Any |
Updated: | 7/16/2013 |
Start Date: | July 2012 |
End Date: | February 2014 |
Contact: | Teva US Medical Information |
Phone: | 800-896-5855 |
Investigation of the Real World Effectiveness of Beclomethasone Dipropionate (BDP) Nasal Aerosol in Perennial Allergic Rhinitis (PAR) Patients
This study will be a prospective observational study of "real world" BDP nasal aerosol users
with PAR, with or without seasonal allergic rhinitis (SAR). Subjects will respond to
monthly online surveys regarding rhinitis control, concomitant medical conditions,
concomitant (non-AR) medications, current AR therapy, and adverse events.
Inclusion Criteria:
- Male or female
- Age 12 years or greater at time of enrollment
- Diagnosis of PAR for at least one year; and 2)a positive skin prick (ie,
epicutaneous) or serum-specific IgE test within the past 2 years to a perennial
allergen as appropriate for the location; and 3)PAR symptoms that are consistent with
exposure to this allergen for at least one year
- Uncontrolled rhinitis symptoms at the time of assessment as confirmed by a score of
21 or less on the RCAT
- Newly prescribed BDP Nasal Aerosol (within the past 7 days but have not yet used)
- Willing and able to complete surveys in English on a computer with internet access
- Willing and able to provide informed consent prior to entering the study (or
parent/caregiver/legal guardian if applicable)
Exclusion Criteria:
- Current acute or chronic sinusitis or chronic purulent nasal discharge
- Rhinitis medicamentosa or nasal structural abnormalities (including nasal polyps and
clinically significant septal deviation) that significantly interfere with nasal
airflow
- Acute upper respiratory infection within the past 14 days
- Used any pressurized metered-dose inhaler INS product (including BDP Nasal Aerosol
and Ciclesonide Nasal Aerosol) within the past 90 days
- Used any experimental therapy for AR within the past 30 days
- Any condition which the investigator feels may interfere with the study
We found this trial at
41
sites
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