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Completed Phase 4 Interventional Results available

Phase 4 Fluticasone Furoate Nasal Spray (VERAMYST) Long Term Pediatric Growth Study.

ClinicalTrials.gov ID: NCT00570492

Public ClinicalTrials.gov record NCT00570492. 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 Nov 1, 2026, 7:40 PM EST

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, Multi-Center Study to Evaluate the Effects of a One-Year Course of Fluticasone Furoate Nasal Spray 110mcg QD on Growth in Pre-Pubescent, Pediatric Subjects With Perennial Allergic Rhinitis

Brief summary

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

The primary objective of this study is to characterize, as accurately as possible, the estimation of the difference in pre-pubescent growth velocities between subjects treated continuously for one year with FFNS 110mcg QD, the highest dose approved for pediatric use in the US, and placebo nasal spray as determined by stadiometry.

Study identification

NCT ID
NCT00570492
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
474 participants

Conditions and interventions

Eligibility (public fields only)

Age range
5 Years to 8 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
Nov 26, 2007 (Type not available)
Primary completion
Mar 1, 2011 (Actual)
Completion
Mar 17, 2011 (Actual)
Last update posted
Sep 15, 2017

2007 – 2011

United States locations

U.S. sites
50
U.S. states
21
U.S. cities
43
Facility City State ZIP Site status
GSK Investigational Site Oxford Alabama 36203 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Rolling Hills Estates California 90274 —
GSK Investigational Site Vista California 92083 —
GSK Investigational Site Coral Gables Florida 33134 —
GSK Investigational Site Ocala Florida 34471 —
GSK Investigational Site Tampa Florida 33613 —
GSK Investigational Site Gainesville Georgia 30501 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Stockbridge Georgia 30281 —
GSK Investigational Site Evansville Indiana 47713 —
GSK Investigational Site Indianapolis Indiana 46208 —
GSK Investigational Site Lenexa Kansas 66215 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Baltimore Maryland 21236 —
GSK Investigational Site Ypsilanti Michigan 48197 —
GSK Investigational Site Plymouth Minnesota 55441 —
GSK Investigational Site Rolla Missouri 65401 —
GSK Investigational Site Warrensburg Missouri 64093 —
GSK Investigational Site Bellevue Nebraska 68123-4303 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Sylvania Ohio 43560 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Oklahoma City Oklahoma 73120 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Portland Oregon 97213 —
GSK Investigational Site Altoona Pennsylvania 16801 —
GSK Investigational Site Pittsburgh Pennsylvania 15212 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Upland Pennsylvania 19013 —
GSK Investigational Site Charleston South Carolina 29414 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site El Paso Texas 79903 —
GSK Investigational Site El Paso Texas 79925 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site Kerrville Texas 78028 —
GSK Investigational Site San Antonio Texas 78205 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Waco Texas 76712 —
GSK Investigational Site South Burlington Vermont 05403 —
GSK Investigational Site Richmond Virginia 23219 —
GSK Investigational Site Richmond Virginia 23229 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00570492, 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 Sep 15, 2017 · Synced Nov 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00570492 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →