Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

Effects of Zoledronic Acid and Raloxifene on Bone Turnover Markers in Postmenopausal Women With Low Bone Mineral Density

ClinicalTrials.gov ID: NCT00431444

Public ClinicalTrials.gov record NCT00431444. 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 24, 2026, 5:45 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 Multi-center, Randomized, Double-blind, Double-dummy Study in Postmenopausal Women With Low Bone Mineral Density to Compare the Effects of a Single Dose of i.v. Zoledronic Acid 5 mg, With Daily Oral Raloxifene 60 mg OD on Bone Turnover Markers

Brief summary

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

This study will compare the effects of Zoledronic acid and Raloxifene in reducing bone turnover markers in postmenopausal women with low bone mineral density over 6 months.

Study identification

NCT ID
NCT00431444
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis
Industry
Enrollment
110 participants

Conditions and interventions

Eligibility (public fields only)

Age range
45 Years to 80 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
Jan 2007 (Type not available)
Primary completion
Jul 2008 (Actual)
Completion
Jul 2008 (Actual)
Last update posted
Mar 29, 2011

2007 – 2008

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
Women's Health Research Phoenix Arizona 85015 —
Associated Pharma Research Center Buena Park California 90620 —
Not listed Washington D.C. District of Columbia 20036 —
Jacksonville Center for Clinical Research Jacksonville Florida 32216 —
Women's Physicians of Jacksonville Jacksonville Florida 32256 —
Tampa Clinical Research Tampa Florida 33624 —
Springfield Clinic Springfield Illinois 62703 —
Consultants in Women's Health Care St Louis Missouri 63131 —
Alegent Health Omaha Nebraska 68152 —
Specialty Medical and Research Center Pahrump Nevada 89048 —
UMDNJ-Robert Wood Johnson Medical Center New Brunswick New Jersey 08901 —
Columbia University New York New York 10032 —
Kernodle Clinic, Inc. Burlington North Carolina 27215 —
The Portland Clinic Portland Oregon 97205 —
Oregon Health and Science University Portland Oregon 97239 —
Texas Institute for Clinical Research Fort Worth Texas 76104 —
Valley Women's Health Clinic Renton Washington 98055 —

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 NCT00431444, 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 Mar 29, 2011 · Synced Oct 24, 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 public registry record, listed eligibility criteria, and available contact information for NCT00431444 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →