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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of the implementation of an educational program on adherence to capecitabine alone or in combination to lapatinib.


Clinical Trial Description

200 subjects who meet the inclusion/exclusion criteria treated by capecitabine +/- lapatinib, will be enrolled into the study. Adherence to treatment of all subjects will be assessed during a first adherence evaluation period of 3 cycles in order to identify patients who need educational intervention(non adherent patients). Only nonadherent patients (adherence rate < 80%) will receive an education intervention. During the educational program, the efficacy of the implementation of an educational program on adherence to capecitabine alone or in combination to lapatinib will be evaluated for the 6 subsequent cycles. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01847599
Study type Interventional
Source Centre Jean Perrin
Contact
Status Terminated
Phase N/A
Start date September 6, 2011
Completion date July 2, 2017

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