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Completed Phase 3 Interventional Results available

3 yr Efficacy & Safety Study of Zoledronic Acid in Post-menopausal Women With Osteoporosis Treated With Zol Acid for 6 Yrs

ClinicalTrials.gov ID: NCT00718861

Public ClinicalTrials.gov record NCT00718861. 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, 6:38 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 3-year, Multicenter, Double-blind, Randomized, Placebo-controlled Extension to CZOL446H2301E1 to Evaluate the Efficacy and Long Term Safety of 6 and 9 Years Zoledronic Acid Treatment of Postmenopausal Women With Osteoporosis

Study identification

NCT ID
NCT00718861
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
190 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Zoledronic acid Drug

Drug

Eligibility (public fields only)

Age range
65 Years and older
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
Mar 31, 2013
Completion
Mar 31, 2013
Last update posted
Oct 8, 2014

2008 – 2013

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
Novartis Investigative Site San Diego California 92103-6204
Novartis Investigative Site Lakewood Colorado 80227
Novartis Investigative Site Gainesville Georgia 30501
Novartis Investigative Site Indiamapolis Indiana 46202
Novartis Investigative Site Bangor Maine 04401
Novartis Investigative Site Albuquerque New Mexico 87106
Novartis Investigative Site Fargo North Dakota 58103
Novartis Investigative Site Pittsburgh Pennsylvania 15261
Novartis Investigative Site Richmond Virginia 23249
Novartis Investigative Site Seattle Washington 98144

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 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00718861, 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 Oct 8, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00718861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →