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Clinical Trial Summary

The main objective of this study is to compare the proportions of late enhancement in patients with Left ventricular (LV) dysfunction as Herceptin ® and in a control group consisting of patients who did not have LV dysfunction after 6 months under the same treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01436604
Study type Interventional
Source Centre Francois Baclesse
Contact
Status Terminated
Phase Phase 2
Start date February 2012
Completion date May 2017

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