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Completed Phase 3 Interventional Results available

Study of an Investigational Nasal Aerosol or Placebo in Children (Ages 4 to 11) With Perennial Allergic Rhinitis (PAR)

ClinicalTrials.gov ID: NCT01783548

Public ClinicalTrials.gov record NCT01783548. 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 Jul 23, 2026, 4:58 PM EDT

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

Official title

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, 12-Week, Clinical Study Designed to Assess the Efficacy and Safety of BDP Nasal Aerosol (80 mcg, Once Daily) in Pediatric Subjects (4 to 11 Years of Age) With PAR

Study identification

NCT ID
NCT01783548
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
547 participants

Conditions and interventions

Interventions

  • BDP Nasal Aerosol Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
4 Years to 11 Years
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
Dec 31, 2012
Primary completion
Sep 30, 2013
Completion
Sep 30, 2013
Last update posted
Oct 11, 2015

2013

United States locations

U.S. sites
63
U.S. states
23
U.S. cities
53
Facility City State ZIP Site status
Teva Investigational Site 10522 Hot Springs Arkansas
Teva Investigational Site 10518 Costa Mesa California
Teva Investigational Site 10526 Downey California
Teva Investigational Site 10496 Huntington Beach California
Teva Investigational Site 10536 Huntington Beach California
Teva Investigational Site 10479 Mission Viejo California
Teva Investigational Site 10524 Orange California
Teva Investigational Site 10508 Paramount California
Teva Investigational Site 10495 San Diego California
Teva Investigational Site 10504 San Diego California
Teva Investigational Site 10505 Stockton California
Teva Investigational Site 10514 Centennial Colorado
Teva Investigational Site 10503 Colorado Springs Colorado
Teva Investigational Site 10499 Lawrenceville Georgia
Teva Investigational Site 10474 Savannah Georgia
Teva Investigational Site 10490 Stockbridge Georgia
Teva Investigational Site 10498 Stockbridge Georgia
Teva Investigational Site 10509 DeKalb Illinois
Teva Investigational Site 10493 Normal Illinois
Teva Investigational Site 10486 Indianapolis Indiana
Teva Investigational Site 10494 Louisville Kentucky
Teva Investigational Site 10515 North Dartmouth Massachusetts
Teva Investigational Site 10540 Traverse City Michigan
Teva Investigational Site 10513 Columbia Missouri
Teva Investigational Site 10532 Missoula Montana
Teva Investigational Site 10507 Brick New Jersey
Teva Investigational Site 10534 Corning New York
Teva Investigational Site 10492 Cortland New York
Teva Investigational Site 10517 Niagara Falls New York
Teva Investigational Site 10482 Rochester New York
Teva Investigational Site 10535 Watertown New York
Teva Investigational Site 10478 High Point North Carolina
Teva Investigational Site 10516 Holly Springs North Carolina
Teva Investigational Site 10485 Canton Ohio
Teva Investigational Site 10480 Cincinnati Ohio
Teva Investigational Site 10500 Cleveland Ohio
Teva Investigational Site 10529 Middleburg Heights Ohio
Teva Investigational Site 10537 Ashland Oregon
Teva Investigational Site 10527 Medford Oregon
Teva Investigational Site 10502 Portland Oregon
Teva Investigational Site 10477 Blue Bell Pennsylvania
Teva Investigational Site 10484 Upland Pennsylvania
Teva Investigational Site 10511 Warwick Rhode Island
Teva Investigational Site 10497 Charleston South Carolina
Teva Investigational Site 10521 Orangeburg South Carolina
Teva Investigational Site 10528 Knoxville Tennessee
Teva Investigational Site 10483 Boerne Texas
Teva Investigational Site 10489 Dallas Texas
Teva Investigational Site 10520 Dallas Texas
Teva Investigational Site 10476 El Paso Texas
Teva Investigational Site 10491 Kerrville Texas
Teva Investigational Site 10487 Plano Texas
Teva Investigational Site 10501 Plano Texas
Teva Investigational Site 10523 San Antonio Texas
Teva Investigational Site 10531 San Antonio Texas
Teva Investigational Site 10539 San Antonio Texas
Teva Investigational Site 10475 Waco Texas
Teva Investigational Site 10488 Salt Lake City Utah
Teva Investigational Site 10506 Salt Lake City Utah
Teva Investigational Site 10510 Salt Lake City Utah
Teva Investigational Site 10519 Burke Virginia
Teva Investigational Site 10481 Richmond Virginia
Teva Investigational Site 10533 Richmond Virginia

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 NCT01783548, 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 Oct 11, 2015 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01783548 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →