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Completed No phase listed Observational

Effectiveness of Beclomethasone Dipropionate Nasal Aerosol for Perennial Allergic Rhinitis

ClinicalTrials.gov ID: NCT01632540

Public ClinicalTrials.gov record NCT01632540. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 12:34 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Investigation of the Real World Effectiveness of Beclomethasone Dipropionate (BDP) Nasal Aerosol in Perennial Allergic Rhinitis (PAR) Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01632540
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
824 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2012
Primary completion
Nov 30, 2013
Completion
Jan 31, 2014
Last update posted
Apr 14, 2014

2012 – 2014

United States locations

U.S. sites
46
U.S. states
21
U.S. cities
42
Facility City State ZIP Site status
Teva Investigational Site 024 Little Rock Alaska
Teva Investigational Site 028 Phoenix Arizona
Teva Investigational Site 003 Encinitas California
Teva Investigational Site 042 Fresno California
Teva Investigational Site 006 Los Angeles California
Teva Investigational Site 017 Orange California
Teva Investigational Site 007 Palmdale California
Teva Investigational Site 021 Paramount California
Teva Investigational Site 040 Redwood City California
Teva Investigational Site 014 Tallahassee Florida
Teva Investigational Site 010 Tamarac Florida
Teva Investigational Site 038 Albany Georgia
Teva Investigational Site 031 Lawrenceville Georgia
Teva Investigational Site 035 Savannah Georgia
Teva Investigational Site 043 Fort Mitchell Kentucky
Teva Investigational Site 034 Owensboro Kentucky
Teva Investigational Site 033 Mandeville Louisiana
Teva Investigational Site 004 Bethesda Maryland
Teva Investigational Site 037 Novi Michigan
Teva Investigational Site 026 Omaha Nebraska
Teva Investigational Site 002 Brick New Jersey
Teva Investigational Site 019 Corning New York
Teva Investigational Site 018 New York New York
Teva Investigational Site 039 Niagara Falls New York
Teva Investigational Site 011 High Point North Carolina
Teva Investigational Site 027 Winston-Salem North Carolina
Teva Investigational Site 030 Winston-Salem North Carolina
Teva Investigational Site 013 Toledo Ohio
Teva Investigational Site 022 Ashland Oregon
Teva Investigational Site 016 Eugene Oregon
Teva Investigational Site 032 Havertown Pennsylvania
Teva Investigational Site 025 Normal Square Pennsylvania
Teva Investigational Site 012 Pittsburgh Pennsylvania
Teva Investigational Site 023 Upland Pennsylvania
Teva Investigational Site 015 Dallas Texas
Teva Investigational Site 029 Dallas Texas
Teva Investigational Site 009 Fort Worth Texas
Teva Investigational Site 020 Houston Texas
Teva Investigational Site 041 San Antonio Texas
Teva Investigational Site 044 San Antonio Texas
Teva Investigational Site 046 San Antonio Texas
Teva Investigational Site 001 Waco Texas
Teva Investigational Site 005 Murray Utah
Teva Investigational Site 045 Newport News Virginia
Teva Investigational Site 008 Puyallup Washington
Teva Investigational Site 036 Greenfield Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01632540, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 14, 2014 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01632540 live on ClinicalTrials.gov.

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