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Completed Phase 4 Interventional Results available

Nasacort AQ Hypothalamic-Pituitary-Adrenal (HPA) Axis Study in Children With Allergic Rhinitis

ClinicalTrials.gov ID: NCT01154153

Public ClinicalTrials.gov record NCT01154153. 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 22, 2026, 2:45 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 Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study Evaluating the Pharmacodynamic Effect of a 6-week Treatment With Triamcinolone Acetonide Aqueous Nasal Spray 110 μg and 220 μg Once Daily on Basal Hypothalamic-Pituitary-Adrenal (HPA) Axis Function in Children [>=2 to < 12 Years of Age] With Allergic Rhinitis (AR).

Study identification

NCT ID
NCT01154153
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Sanofi
Industry
Enrollment
140 participants

Conditions and interventions

Interventions

  • Placebo nasal spray Drug
  • Triamcinolone acetonide aqueous (TAA-AQ) nasal spray (NASACORT AQ) Drug
  • Claritin® Syrup Drug

Drug

Eligibility (public fields only)

Age range
2 Years to 12 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
May 31, 2010
Primary completion
Sep 30, 2010
Completion
Sep 30, 2010
Last update posted
Jun 25, 2012

2010

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Investigational Site Number 840003 Cypress California 90630
Investigational Site Number 840006 Stockbridge Georgia 30281
Investigational Site Number 840007 North Dartmouth Massachusetts 02747
Investigational Site Number 840010 Plymouth Minnesota 55441
Investigational Site Number 840001 Omaha Nebraska 68144
Investigational Site Number 840008 Raleigh North Carolina 27607
Investigational Site Number 840002 Spartanburg South Carolina 29307
Investigational Site Number 840005 San Antonio Texas 78229

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 NCT01154153, 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 Jun 25, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01154153 live on ClinicalTrials.gov.

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