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Hemostatic Profiles of Endocrine Therapies for Breast Cancer — HEMOBREAST  

Breast Neoplasms Clinical Trial

Official title:
Hemostatic Profiles Associated With Use of Aromatase Inhibitors and Tamoxifen in Women With Breast Cancer : a Prospective Cohort Study

Clinical Trial Summary

The aim of this prospective cohort study is to evaluate the modifications of the biological hemostatic profile associated with the use of endocrine therapy in women with breast cancer (tamoxifen or aromatase inhibitors).

Clinical Trial Description

In this cohort study, women with breast cancer and an indication for endocrine therapy will be prospectively enrolled. At the 1st visit (before the start of endocrine therapy (tamoxifen or aromatase inhibitor)) and at the 2nd visit (at ~3 months after the start of treatment), demographical / clinical data and blood samples will be collected. We will evaluate the hemostatic biological profiles associated with the use of endocrine therapy by comparing hemostatic biomarkers before and during its use. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03381963
Study type Observational
Source University Hospital, Geneva
Contact
Status Completed
Phase
Start date April 1, 2017
Completion date February 28, 2020
View Details
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