Clinical Trials Directory

Trials / Terminated

TerminatedNCT00391950

Maintaining Bone Strength in Men With Prostate Cancer

An Open-Label, Randomized, Multicentre Study to Evaluate the Efficacy of Two Zoledronic Acid Schedules on Bone Mineral Density in Prostate Cancer Patients Undergoing Androgen Deprivation Therapy

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Novartis · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to see if giving zoledronic acid three times a year is as effective as five times a year, in increasing bone strength in men with prostate cancer. All participants will receive the active drug but half will receive drug every 6 months and the other half will receive drug every 3 months. Both patient and doctor will know which treatment a patient is receiving. After 1 year of treatment bone strength will be measured with scans and compared to the strength at the start of the study. All participants will stop receiving the drug after 1 year and will be seen back in the clinic, annually for another 2 years for follow-up.

Conditions

Interventions

TypeNameDescription
DRUGZoledronic acid

Timeline

Start date
2006-10-01
Primary completion
2007-05-01
First posted
2006-10-25
Last updated
2009-11-23

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00391950. Inclusion in this directory is not an endorsement.