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Clinical Trial Summary

The primary objective of this study is to evaluate the impact of the result of the Prosigna Test (assay) on the therapeutic decision of adjuvant therapy (chemotherapy and hormone therapy) in patients suffering from early-stage breast cancer.


Clinical Trial Description

The secondary objectives will consist of:

- The evaluation of the confidence in the therapeutic indications of the practitioners before and after the test (assay) results, and by subgroups of cancers

- The evaluation of the rate of secondary effects of chemotherapy,

- The evaluation of the emotional state of patients faced with the therapeutic decision, of their degree of anxiety and of their functional status before and after the Prosigna test (assay) results ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02395575
Study type Observational
Source NanoString Technologies, Inc.
Contact
Status Completed
Phase N/A
Start date March 2015
Completion date October 2017

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