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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 Oct 19, 2026, 2:00 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

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 28, 2014 (Actual)
Primary completion
Mar 26, 2018 (Actual)
Completion
Mar 26, 2018 (Actual)
Last update posted
Apr 10, 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 10, 2019 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01957150 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →