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ClinicalTrials.gov record
Completed Phase 4 Interventional

Study Of Asthma And Genetics In Patients To Be Treated With Fluticasone Propionate/Salmeterol Or Salmeterol Xinafoate

ClinicalTrials.gov ID: NCT00102882

Public ClinicalTrials.gov record NCT00102882. 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 Oct 26, 2026, 7:34 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

Randomized, Double-Blind Comparison of Advair 100/50 BID vs Salmeterol BID vs Albuterol QID in Subjects With ARG/ARG Genotype 12 Years of Age and Older With Presistent Asthma on Short-Acting Beta2-Agonists Alone

Brief summary

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

This study may last up to 36-38 weeks. Patients will visit the clinic 11 times. A blood sample will be taken at Visit 1 to look at subjects' genes. Breathing tests will be done during the study. Study medicines and procedures will be provided at no cost. Patients will be treated with VENTOLIN (8 wks), ATROVENT (8 wks), then ADVAIR or SEREVENT (16 wks). ADVAIR and SEREVENT are FDA approved for the treatment of asthma in patients 4 years of age and older.

Study identification

NCT ID
NCT00102882
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
547 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
Oct 2004 (Type not available)
Primary completion
Jan 2007 (Actual)
Completion
Jan 2007 (Actual)
Last update posted
Feb 3, 2017

2004 – 2007

United States locations

U.S. sites
86
U.S. states
29
U.S. cities
73
Facility City State ZIP Site status
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Inglewood California 90301 —
GSK Investigational Site Irvine California 92618 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Spring Valley California 91978 —
GSK Investigational Site Stockton California 95207 —
GSK Investigational Site Colorado Springs Colorado 80907 —
GSK Investigational Site Denver Colorado 80206 —
GSK Investigational Site Denver Colorado 80209 —
GSK Investigational Site Lakewood Colorado 80401 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Waterbury Connecticut 06708 —
GSK Investigational Site Coral Gables Florida 33134 —
GSK Investigational Site Jacksonville Florida 32207 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Miami Florida 33176 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Sarasota Florida 34233 —
GSK Investigational Site South Miami Florida 33143 —
GSK Investigational Site Tallahassee Florida 32308 —
GSK Investigational Site Tampa Florida 33613 —
GSK Investigational Site Atlanta Georgia 30310 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Lilburn Georgia 30047 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Indianapolis Indiana 46208 —
GSK Investigational Site Overland Park Kansas 66210 —
GSK Investigational Site Covington Louisiana 70433 —
GSK Investigational Site Metairie Louisiana 70002 —
GSK Investigational Site Shreveport Louisiana 71104 —
GSK Investigational Site Shreveport Louisiana 71105 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Baltimore Maryland 21237 —
GSK Investigational Site Boston Massachusetts 02118 —
GSK Investigational Site North Dartmouth Massachusetts 02747 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site Columbia Missouri 65203 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Warrensburg Missouri 64093 —
GSK Investigational Site Papillion Nebraska 68046 —
GSK Investigational Site Hackensack New Jersey 07601 —
GSK Investigational Site Newark New Jersey 07103-2499 —
GSK Investigational Site Bay Shore New York 11706 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site Rochester New York 14618 —
GSK Investigational Site Asheville North Carolina 28801 —
GSK Investigational Site Winston-Salem North Carolina 27157 —
GSK Investigational Site Oklahoma City Oklahoma 73120 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Philadelphia Pennsylvania 19143 —
GSK Investigational Site Upland Pennsylvania 19013 —
GSK Investigational Site Charleston South Carolina 29407 —
GSK Investigational Site Charleston South Carolina 29414 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Chattanooga Tennessee 37421 —
GSK Investigational Site Knoxville Tennessee 37920 —
GSK Investigational Site Nashville Tennessee 37203-1424 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site El Paso Texas 79902 —
GSK Investigational Site El Paso Texas 79925 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site Kerrville Texas 78028 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site South Burlington Vermont 05403 —
GSK Investigational Site Richmond Virginia 23229 —
GSK Investigational Site Bellingham Washington 98225 —
GSK Investigational Site Kirkland Washington 98034 —
GSK Investigational Site Madison Wisconsin 53792 —
GSK Investigational Site Milwaukee Wisconsin 53209-0996 —
GSK Investigational Site Milwaukee Wisconsin 53219 —
GSK Investigational Site Milwaukee Wisconsin 53226 —
GSK Investigational Site West Allis Wisconsin 53227 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00102882, 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 Feb 3, 2017 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00102882 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →