Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00046254 · ClinicalTrials.gov registry record · Phase 3

Evaluating the Ability of Zoledronic Acid to Reduce the Rate of Subsequent Osteoporotic Fractures After a Hip Fracture

A Phase 3 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
2,127
Enrollment target

NCT00046254 is a Phase 3 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 2,127 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00046254, a Phase 3 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
2,127 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate whether zoledronic acid given once yearly for two years to men and women after surgical repair of a recent hip fracture will significantly reduce the rate of all re-occurring (new) osteoporotic fractures. All patients will receive vitamin D and calcium.

Interventions

  • DRUG Zoledronic Acid

Trial Details

FieldValue
Enrollment Target 2,127 participants
Start Date 2002-02
Est. Completion 2007-02
Phase Phase 3

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT00046254

The ClinicalTrials.gov registry entry for NCT00046254 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 2,127 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Zoledronic Acid is the first listed.

NCT00046254 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00046254 about?

NCT00046254 is a clinical study titled "Evaluating the Ability of Zoledronic Acid to Reduce the Rate of Subsequent Osteoporotic Fractures After a Hip Fracture". The purpose of this study is to evaluate whether zoledronic acid given once yearly for two years to men and women after surgical repair of a recent hip fracture will significantly reduce the rate of all re-occurring (new) osteoporotic fractures. All patients will receive vitamin D and calcium.

What is the current status of trial NCT00046254?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 2,127 participants. The study started on 2002-02. Estimated completion is 2007-02.

What interventions are being tested in trial NCT00046254?

The interventions under investigation include: Zoledronic Acid (DRUG).

Who is sponsoring clinical trial NCT00046254?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.