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Completed Phase 4 Interventional Results available

Efficacy of Pioglitazone on Bone Metabolism in Postmenopausal Women With Impaired Fasting Glucose.

ClinicalTrials.gov ID: NCT00708175

Public ClinicalTrials.gov record NCT00708175. 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 Jul 22, 2026, 7:37 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 Phase 4, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of Pioglitazone Compared to Placebo on Bone Metabolism in Impaired Fasting Glucose, Postmenopausal Women for One Year of Treatment

Study identification

NCT ID
NCT00708175
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Takeda
Industry
Enrollment
156 participants

Conditions and interventions

Interventions

  • Pioglitazone Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
Up to 70 Years
Sex
Female
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
Apr 30, 2008
Primary completion
Dec 31, 2010
Completion
Jan 31, 2011
Last update posted
Feb 2, 2012

2008 – 2011

United States locations

U.S. sites
34
U.S. states
22
U.S. cities
34
Facility City State ZIP Site status
Not listed Greenbrae California
Not listed Los Banos California
Not listed San Diego California
Not listed Walnut Creek California
Not listed West Hills California
Not listed Lakewood Colorado
Not listed Longmont Colorado
Not listed Boynton Beach Florida
Not listed Hialeah Florida
Not listed Jupiter Florida
Not listed Dunwoody Georgia
Not listed Gainesville Georgia
Not listed Honolulu Hawaii
Not listed Idaho Falls Idaho
Not listed Chicago Illinois
Not listed Des Moines Iowa
Not listed Iowa City Iowa
Not listed Louisville Kentucky
Not listed Metarie Louisiana
Not listed Scarborough Maine
Not listed Bethesda Maryland
Not listed Detroit Michigan
Not listed Omaha Nebraska
Not listed Albuquerque New Mexico
Not listed Mineola New York
Not listed West Haverstraw New York
Not listed Pinehurst North Carolina
Not listed Cincinnati Ohio
Not listed Portland Oregon
Not listed Aiken South Carolina
Not listed Greenville South Carolina
Not listed Brentwood Tennessee
Not listed Denton Texas
Not listed Houston Texas

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00708175, 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 2, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00708175 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →