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

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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
2305
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Tamarac, FL
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1964
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Albany, GA
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616
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Ashland, OR
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Bethesda, Maryland
2277
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Bethesda, MD
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2428
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Brick, NJ
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Corning, New York
2272
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Corning, NY
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1224
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Dallas, TX
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Encinitas, California
82
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Encinitas, CA
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740
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Eugene, OR
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Fort Mitchell, Kentucky
1877
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Fort Mitchell, KY
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Fort Worth, Texas
1194
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Fort Worth, TX
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Fresno, California
209
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Fresno, CA
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Greenfield, Wisconsin
1723
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Greenfield, WI
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Havertown, Pennsylvania
2367
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Havertown, PA
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High Point, North Carolina
2141
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High Point, NC
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Houston, Texas 77054
1358
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from 91732
Houston, TX
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Lawrenceville, Georgia
1939
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Lawrenceville, GA
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Little Rock, Alaska
1463
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Little Rock, AK
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Los Angeles, California
13
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Los Angeles, CA
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Mandeville, Louisiana
1647
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Mandeville, LA
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565
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Murray, UT
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New York, New York
2432
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New York, NY
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Newport News, Virginia
2324
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Newport News, VA
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Niagara Falls, New York
2172
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Niagara Falls, NY
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Normal, Pennsylvania
2149
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Normal, PA
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1946
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Novi, MI
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1300
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Omaha, NE
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Orange, California
21
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Orange, CA
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Owensboro, Kentucky
1739
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Owensboro, KY
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Palmdale, California
35
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Palmdale, CA
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Paramount, California
15
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Paramount, CA
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Phoenix, Arizona
343
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Phoenix, AZ
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Pittsburgh, Pennsylvania
2119
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Pittsburgh, PA
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Puyallup, Washington
933
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Puyallup, WA
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Redwood City, California
333
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Redwood City, CA
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San Antonio, Texas
1188
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San Antonio, TX
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Savannah, Georgia 31406
2131
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Savannah, GA
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Tallahassee, Florida
1977
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Tallahassee, FL
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1937
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Toledo, OH
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Upland, Pennsylvania
2343
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Upland, PA
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Winston-Salem, North Carolina 27103
2123
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Winston-Salem, NC
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