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Completed Phase 3 Interventional

A Study of the Clinical Safety, Tolerability, and Efficacy of Zoledronic Acid Compared to an Oral Bisphosphonate

ClinicalTrials.gov ID: NCT00100555

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00100555. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 15, 2026, 2:30 PM EST

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Brief summary

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

The purpose of this trial is to study the clinical safety, tolerability, and efficacy of zoledronic acid compared to an oral bisphosphonate in postmenopausal women with osteoporosis.

Study identification

NCT ID
NCT00100555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
120 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
45 Years to 79 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
Jun 2004 (Type not available)
Primary completion
Jun 2005 (Actual)
Completion
Jun 2005 (Actual)
Last update posted
Apr 27, 2012

2004 – 2005

United States locations

U.S. sites
18
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
Univ. of Alabama/Division of Clinical Immunology and Rheumatology Birmingham Alabama 35294 —
Radiant Research San Diego California 92108 —
Denver Arthritis Clinic Denver Colorado 80230 —
Florida Medical Research Institute Gainesville Florida 32605 —
Northwestern Center for Clinical Research Chicago Illinois 60611 —
The Center for Rheumatology and Bone Research Wheaton Maryland 20902 —
Midwest Arthritis Center Kalamazoo Michigan 49048-1634 —
St. John's Medical Research Springfield Missouri 65807 —
Deaconess Billings Clinic Research Division Billings Montana 59101 —
UMDNJ-Robert Wood Johnson Medical School New Brunswick New Jersey 08903 —
Helen Hayes Hospital - Regional Bone Clinic West Haverstraw New York 10993 —
Private Practice Mayfield Village Ohio 44143 —
The Arthritis Clinic of Jackson Jackson Tennessee 38305 —
Radiant Research Dallas Texas 75235 —
Univ. of North Texas Health Science Center at Fort Worth Fort Worth Texas 76107 —
St. Luke's Episcopal Hospital Ctr for Ortho. Res. and Education Houston Texas 77030 —
Women's Health Center Salt Lake City Utah 84117 —
Valley Medical Associates Lewisburg West Virginia 24901 —

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 NCT00100555, 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 27, 2012 · Synced Nov 15, 2026

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