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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 Oct 30, 2026, 9:03 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

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

Brief summary

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

The purpose of this study is to evaluate the effect of pioglitazone on bone metabolism in postmenopausal women with impaired fasting glucose.

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

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
May 2008 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Feb 2011 (Actual)
Last update posted
Feb 3, 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 3, 2012 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00708175 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →