Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A 24-week Arterial Stiffness Study With Fluticasone Furoate/Vilanterol in COPD

ClinicalTrials.gov ID: NCT01336608

Public ClinicalTrials.gov record NCT01336608. 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 4, 2026, 10:55 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

A 24-week Study to Evaluate the Effect of Fluticasone Furoate/Vilanterol 100/25 mcg Inhalation Powder Delivered Once-daily Via a Novel Dry Powder Inhaler on Arterial Stiffness Compared With Placebo and Vilanterol in Subjects With Chronic Obstructive Pulmonary Disease (COPD).

Brief summary

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

The purpose of the study is to investigate the effect of fluticasone furoate/vilanterol Inhalation Powder on arterial stiffness compared with placebo and vilanterol over a 24-week treatment period in subjects with COPD and aortic pulse wave velocity of 11.0 m/s or above.

Study identification

NCT ID
NCT01336608
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
446 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 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
Mar 3, 2011
Primary completion
Nov 3, 2014
Completion
Nov 3, 2014
Last update posted
Nov 7, 2017

2011 – 2014

United States locations

U.S. sites
36
U.S. states
19
U.S. cities
36
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294
GSK Investigational Site Phoenix Arizona 85006
GSK Investigational Site Newport Beach California 92663
GSK Investigational Site Torrance California 90505
GSK Investigational Site DeLand Florida 32720
GSK Investigational Site Gainesville Florida 32608
GSK Investigational Site Orlando Florida 32825
GSK Investigational Site Ormond Beach Florida 32174
GSK Investigational Site Winter Park Florida 32789
GSK Investigational Site Duluth Georgia 30096
GSK Investigational Site Coeur d'Alene Idaho 83814
GSK Investigational Site Avon Indiana 46123
GSK Investigational Site Lafayette Indiana 47904
GSK Investigational Site Muncie Indiana 47304-5547
GSK Investigational Site Topeka Kansas 66606
GSK Investigational Site Traverse City Michigan 49684
GSK Investigational Site Saint Charles Missouri 63301
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Charlotte North Carolina 28207
GSK Investigational Site Shelby North Carolina 28152
GSK Investigational Site Winston-Salem North Carolina 27103
GSK Investigational Site Columbus Ohio 43215
GSK Investigational Site Oklahoma City Oklahoma 73103
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Pittsburgh Pennsylvania 15213
GSK Investigational Site Easley South Carolina 29640
GSK Investigational Site Fort Mill South Carolina 29707
GSK Investigational Site Gaffney South Carolina 29340
GSK Investigational Site Greenville South Carolina 29615
GSK Investigational Site Rock Hill South Carolina 29732
GSK Investigational Site Seneca South Carolina 29678
GSK Investigational Site Spartanburg South Carolina 29303
GSK Investigational Site Union South Carolina 29379
GSK Investigational Site Johnson City Tennessee 37601
GSK Investigational Site Edinburg Texas 78539
GSK Investigational Site Abingdon Virginia 24210

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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01336608, 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 Nov 7, 2017 · Synced Sep 4, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01336608 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →