Study identifier:NIS-OSI-DUM-2008/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An open label non-interventional evaluation of the effect of adjuvant hormonal treatment of postmenopausal women wih early breast cancer with aromatase inhibitors on bone mineral density and bone fracture rate in daily practice
Breast Cancer
-
No
-
Female
560
Observational
55 Years - 65 Years
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
The aim of this study is to determine the effect of aromatase inhibitors therapy on bone mineral density and compare it to the effects of tamoxifen and no hormonal therapy.
Location
Location
Ljubljana, Slovenia
Arms | Assigned Interventions |
---|---|
A: 70 women with hormone-dependent or hormone-independent early breast cancer that have completed their chemo- and/or radiotherapy just recently (up to 6 months after completion of therapy) | - |
B 70 women with hormone-independent early breast cancer, 24-36 months after completion of chemo- and/or radiotherapy | - |
C 70 women with hormone-independent early breast cancer, 54-66 months after completion of chemo- and/or radiotherapy | - |
D 70 women with hormone-dependent early breast cancer, 24-36 months after initiation of tamoxifen therapy | - |
E 70 women with hormone-dependent early breast cancer, 24-36 months after initiation of aromatase inhibitors therapy | - |
F 70 women with hormone-dependent early breast cancer, 54-66 months after initiation of tamoxifen therapy | - |
G 70 women with hormone-dependent early breast cancer, 54-66 months after initiation of aromatase inhibitors therapy | - |
H 70 women with hormone-dependent early breast cancer, 24-36 months after initiation of aromatase inhibitors therapy following 24-36 months of initial tamoxifen therapy | - |
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