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Completed Phase 4 Interventional Results available

Study Evaluating the Effect of Fluticasone Furoate/ Vilanterol (FF/VI) Inhalation Powder Compared With Vilanterol (VI) Inhalation Powder on Bone Mineral Density (BMD) in Subjects With Chronic Obstructive Pulmonary Disease (COPD).

ClinicalTrials.gov ID: NCT01957150

Public ClinicalTrials.gov record NCT01957150. 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 2, 2026, 4:24 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

Multi-centre, Randomized, Double-blind, Parallel-group Study Evaluating the Effect of Fluticasone Furoate/ Vilanterol (FF/VI) Inhalation Powder Once Daily Compared With Vilanterol (VI) Inhalation Powder Once Daily on Bone Mineral Density (BMD) in Subjects With Chronic Obstructive Pulmonary Disease (COPD).

Brief summary

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

This is a multi-center, randomized, double-blind, parallel-group study. The FF/VI inhalation powder once daily and VI inhalation powder once daily will be evaluated in subjects with COPD over 156 weeks. The primary objective of this study is to evaluate the effect of the inhaled corticosteroid FF on bone mineral density assessed at the total hip by comparing FF/VI treatment with VI treatment in subjects with moderate COPD.

Study identification

NCT ID
NCT01957150
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
283 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
Jan 27, 2014
Primary completion
Mar 25, 2018
Completion
Mar 25, 2018
Last update posted
Apr 9, 2019

2014 – 2018

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
GSK Investigational Site Jasper Alabama 35501
GSK Investigational Site Phoenix Arizona 85006
GSK Investigational Site Fort Lauderdale Florida 33316
GSK Investigational Site Lawrenceville Georgia 30046
GSK Investigational Site Minneapolis Minnesota 55402
GSK Investigational Site Plymouth Minnesota 55441
GSK Investigational Site Bellevue Nebraska 68123-4303
GSK Investigational Site Wilmington North Carolina 28401
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Erie Pennsylvania 16508
GSK Investigational Site Charleston South Carolina 29406-7108
GSK Investigational Site Old Point Station South Carolina 29707
GSK Investigational Site Spartanburg South Carolina 29303
GSK Investigational Site Chattanooga Tennessee 37404
GSK Investigational Site Knoxville Tennessee 37919
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Spokane Valley Washington 99216

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 28 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01957150, 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 Apr 9, 2019 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01957150 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →