Clinical Trials Directory

Trials / Completed

CompletedNCT00784940

ATAC - Bone Density Sub-Protocol

A Randomised, Double-Blind Trial to Assess the Effects on Bone Mineral Density and Metabolism of Arimidex Alone, Nolvadex Alone, or Arimidex and Nolvadex in Combination, (in Comparison to a Control Group) When Used as Adjuvant Treatment for Breast Cancer in Postmenopausal Women

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
308 (actual)
Sponsor
AstraZeneca · Industry
Sex
Female
Age
45 Years
Healthy volunteers
Not accepted

Summary

To assess and quantify the changes in bone mineral density between the ARIMIDEX and ARIMIDEX plus NOLVADEX groups when compared to the NOLVADEX alone treatment group whilst receiving trial therapy.

Conditions

Interventions

TypeNameDescription
DRUGAnastrozole1mg, orally, once daily
DRUGTamoxifen20mg, orally, once daily

Timeline

Start date
1998-06-01
Primary completion
2005-03-01
Completion
2007-04-01
First posted
2008-11-04
Last updated
2009-04-27

Source: ClinicalTrials.gov record NCT00784940. Inclusion in this directory is not an endorsement.

ATAC - Bone Density Sub-Protocol (NCT00784940) · Clinical Trials Directory